Composition comprising a progenitor/precursor cell population

ABSTRACT

A population of cultured cells is provided that comprises at least 10% of a sub-population of cells that: stain as CD31 Bright, demonstrate uptake of Ac-LDL+, and secrete both IL-8 and angiogenin.

CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a §371 national stage of PCT International Application No. PCT/IL2007/000308, filed Mar. 8, 2007, and claims the benefit of U.S. Provisional Application No. 60/780,781, filed Mar. 8, 2006, the contents of all of which are hereby incorporated by reference into this application.

FIELD OF THE INVENTION

The present invention generally relates to regulating stem cells. Specifically, the present invention relates to the induction of migration and differentiation of stem cells.

BACKGROUND OF THE INVENTION

Since the discovery of stem cells, it has been understood that they have significant potential to effectively treat many diseases [1]. Pluripotent stem cells derived from embryos and fetal tissue have the potential to produce more than 200 different known cell types, and thus can potentially replace dying or damaged cells of any specific tissue [2, 3]. Stem cells differ from other types of cells in the body, and, regardless of their source, have three general properties: (a) they are capable of dividing and renewing themselves for long periods, (b) they are undifferentiated, and (c) they can give rise to specialized cell types.

Stem cells have been identified in most organs and tissues, and can be found in adult animals and humans. Committed adult stem cells (also referred as somatic stem cells) were identified long ago in bone marrow. In the past decade, committed adult stem cells have also been identified in tissues that were previously not thought to contain them, such as brain tissue, skin tissue, and skeletal muscle tissue [8, 9, 10, 11, 12, 13]. It was initially believed that adult stem cells are tissue-committed cells that can only differentiate into cells of the same tissue and thus regenerate the damaged tissue [1, 4, 5, 6, 7]. However, recent work suggests that adult organ-specific stem cells are capable of differentiating into cells of different tissues [8, 9, 10, 11, 14, 16]. Transplantation of cells derived from brain, muscle, skin and fat tissue has been shown to result in a detectable contribution in several lineages distinct from their tissue of origin [8, 9, 10, 11]. For example, recent reports support the view that cells derived from hematopoietic stem cells (HSCs) can differentiate into cells native to the adult brain [14], providing additional evidence for the plasticity of such stem cells.

The HSC is the best characterized stem cell. This cell, which originates in bone marrow, peripheral blood, cord blood, the fetal liver, and the yolk sac, generates blood cells and gives rise to multiple hematopoietic lineages. As early as 1998, researchers reported that pluripotent stem cells from bone marrow can, under certain conditions, develop into several cell types different from known hematopoietic cells [13, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27]. Such an ability to change lineage is referred to as cellular transdifferentiation or cell plasticity. Bone marrow-derived stem cells (BMSCs) have already been shown to have the ability to differentiate into adipocytes, chondrocytes, osteocytes, hepatocytes, endothelial cells, skeletal muscle cells, and neurons [28, 29, 30, 31, 32].

The process of stem cell differentiation is controlled by internal signals, which are activated by genes within the cell, and by external signals for cell differentiation that include chemicals secreted by other cells, physical contact with neighboring cells, and certain molecules in the microenvironment [33, 34]. For example, if embryonic stem cells are allowed to aggregate to form embryoid bodies, they begin to differentiate spontaneously. Embryonic cells of embryoid bodies can form muscle cells, nerve cells, and many other cell types [35, 36]. Although spontaneous differentiation is a good indication that a culture of embryonic stem cells is healthy, it is not an efficient way to produce cultures of specific cell types. In order to generate cultures of specific types of differentiated cells, e.g., myocytes, blood cells, or nerve cells, scientists must control the multiplication and the differentiation of stem cells by regulating the chemical composition of the culture medium, altering the surface of the culture dish, and/or by inserting specific genes.

Successful attempts have been made in vitro to induce differentiation of adult stem cells into other cells by co-culturing with other adult cells. For example, recent work has shown that co-culturing adult mouse BMSCs and embryonic heart tissue causes the BMSCs to both integrate into cardiac tissue and differentiate into cardiomyocytes (CMCs). Other work has shown that mesenchymal stem cells acquire characteristics of cells in the periodontal ligament when co-cultured with periodontal ligament tissue [37, 38].

Tissue injury may be one of the stimulants for the recruitment of stem cells to an injured site, by causing changes in the tissue environment, thereby drawing stem cells from peripheral blood, as well as triggering tissue replacement by locally resident stem cells. Some reports of elevated levels of chemokines and chemokine receptors such as CXCR4-SDF explain some of this in vivo stem cell recruitment [39]. Other reports suggest an important role of the chemokine CXCR8 (IL-8) as an anti-apoptotic agent which promotes tissue survival and induces recruitment of endogenous stem/progenitor cells [M, N, O]. An example of this mechanism can be seen in recent work showing that stem cells differentiate into liver cells when co-cultured with injured liver cells separated from the stem cells by a barrier [30].

CD31, the platelet endothelial cell adhesion molecule-1 (PECAM-1), is widely used as a marker during the development of endothelial cell progenitors, vasculogenesis and angiogenesis (A, B, C, D, E, F, H1). CD31 is constitutively expressed on the surface of adult and embryonic endothelial cells, is a major constituent of the endothelial cell intercellular junction (where up to 10^6 PECAM-1 molecules are concentrated) and is weakly expressed on many peripheral leukocytes and platelets (E, G, H). With a few minor exceptions, CD31 is not present on fibroblasts, epithelium, muscle, or other nonvascular cells. Independently of CD31 expression, endothelial cells and their progenitors are typically characterized by binding of Ulex-lectin in combination with the ability to uptake Acetylated-Low Density Lipoprotein (Ac-LDL) (I).

Regenerative medicine is an emerging scientific field with implications for both basic and practical research. Stem and progenitor cells are applied in a form of cellular therapy for local tissue repair and regeneration [41, 42]. These treatments aim to treat disorders in practically all tissues and organs, such as the bladder, intestine, kidney, trachea, eye, heart valves, and bones [43, 44]. Intensive studies are being conducted worldwide in order to generate stem cell-based tissue engineering therapies. These studies include experiments for the regeneration of blood vessels [13], bone [35, 45], cartilage, cornea, dentin, heart muscle [46], liver, pancreas [47], nervous tissue, skeletal muscle, and skin [18, 34, 48, 49]. Stem cell-based therapies can use cells from various organs in order to generate different tissues. For example, epithelial surfaces (taken from various tissues such as the skin, cornea and mucosal membrane) may be used as a source for corneal and skeletal tissues [50, 51]. Additionally, in a more widespread application, blood marrow-derived stern cells are used for regeneration of several different tissues such as bone, cartilage, adipocytes, neurons, and cells of the hematopoietic system [33, 42].

Stem cells can be administrated systemically or locally using injections to the injured site. However, other potential administration routes and usage of different medical devices are being developed and tested. Different medical devices such as chemical, metal or biodegradable based devices have been described for the administration of stem cells into the heart and blood vessels (J, K).

US Patent Application Publication 2004/0228847 to Goldschmidt-Clermont et al., which is incorporated herein by reference, describes stem/progenitor cells and, in particular, therapeutic strategies based on the use of such cells to effect vascular rejuvenation and/or to serve as delivery vehicles.

PCT Patent Publication WO 2005/120090 to Fulga et al., which is assigned to the assignee of the present patent application and is incorporated herein by reference, describes a method for use with extracted blood, including (a) applying blood to a first gradient suitable for selecting first-pass cells having a density less than 1.077 g/ml; (b) applying the first-pass cells to a second gradient suitable for selecting second-pass cells having a density between 1.055 and 1.074 g/ml; (c) increasing the number of cells having a density between 1.055 and 1.074 g/ml, by culturing the second-pass cells for a period lasting between 3 and 30 days; and (d) identifying endothelial progenitor cells in the cultured cells. Other embodiments are also described.

United States Patent Application Publication 2004-0228897 to Zhang et al., which is incorporated herein by reference, describes a medical device for use to assist stem cell and/or stem cell derivatives in repopulating, repairing and/or replacing the heart tissue in a failing heart muscle, in order to restore the heart's ability to pump blood. The medical device is made of biocompatible materials. The specific design of the device is described as facilitating the stem cells coated in the device to repopulate heart muscles inside the heart. Stem cells are attached to the coated device, proliferated and/or differentiated on the device in a bioreactor before implantation. The device also contains bioactive components that diminish rejection by the host's immune system. The device may be directly implanted into the failing heart muscle area to assist stem cells to repair failing heart muscles via surgical and/or percutaneous catheter based procedures. In another embodiment, the device may be implanted to the surgical site where abnormal heart muscles are removed, to assist stem cells to repopulate heart muscles, to replace the failing heart muscles.

US Patent Application Publication 2005/0209556 to Tresco et al., which is incorporated herein by reference, describes a device and method for the delivery of cells, tissues, enzymes and/or pharmacological agents for the treatment or prevention of diseases, disorders or deficiencies. The device is placed intravascularly and includes a chamber that houses living cells delimited by a membrane on either side that physically separates the cells from the blood stream and the central lumen of the catheter. The device can be inserted over a guidewire and permits flushing and reloading of the central lumen with viability supporting factors that sustain the cells in the outer chamber for long indwelling times without removing it from the body. In addition, the central lumen can be used to deliver therapeutic substances or withdraw blood. The new intravascular catheter is described as being able to be used for the treatment or prevention of a variety of diseases and disorders, and may use the implantation of living cells, tissues, enzymes or pharmacological agents. The device is described as being used, for example, for non-therapeutic purposes that may involve sustained intravascular release of biological factors as, for example, in stimulating growth of farm animals to augment the production of meat. Placement of cells within the device for release of angiogenesis, cytokines, enzymes, and other factors is described. The use of stem cells within the device is also described.

U.S. Pat. No. 6,810,286 to Donovan et al., which is incorporated herein by reference, describes a stimulatory device for the controlled production of angiogenic growth factors. More specifically, a subthreshold pulse generator is used for the local production of vascular endothelial growth factor.

The following references, which are incorporated herein by reference, may be of interest:

1. Leblond C. P. (1964), “Classification of cell populations on the basis of their proliferative behaviour,” Natl. Cancer Inst. Monogr. 14:119-150

2. Evans M. J. and Kaufman M. H. (1981), “Establishment in culture of pluripotential cells from mouse embryos,” Nature 292:154-156

3. Donovan P. J. and Gearhart J. (2001), “The end of the beginning for pluripotent stem cells,” Nature 414:92-97

4. Spradling A. et al. (2001), “Stem cells find their niche,” Nature 414:98-104

5. Weissman I. L. et al. (2001), “Stem and progenitor cells: origins, phenotypes, lineage commitments, and transdifferentiations,” Annu. Rev. Cell. Dev. Biol. 17:387-403

6. Weissman I. L. (2000), “Stem cells: units of development, units of regeneration, and units in evolution,” Cell 100:157-68

7. Cheng A, Wang S, Cai J, Rao M S, Mattson M P (2003), “Nitric oxide acts in a positive feedback loop with BDNF to regulate neural progenitor cell proliferation and differentiation in the mammalian brain,” Dev Biol. 258(2):319-33

8. Cousin B, Andre M, Arnaud E, Penicaud L, Casteilla L (2003), “Reconstitution of lethally irradiated mice by cells isolated from adipose tissue,” Biochem Biophys Res Commun. 301(4):1016-22

9. Anderson D. J., Gage, F. H., and Weissman, I. L. (2001), “Can stem cells cross lineage boundaries?” Nat. Med. 7:393-395

10. Robey P. G. (2000), “Stem cells near the century mark,” J. Clin. Invest. 105:1489-1491

11. Eisenberg L M, Burns L, Eisenberg C A (2003), “Hematopoietic cells from bone marrow have the potential to differentiate into cardiomyocytes in vitro,” Anat Rec. 274A(1):870-82

12. Karl J. L., Fernandes Ian A. McKenzie, Pleasantine Mill et al. (2004), “A dermal niche for multipotent adult skin-derived precursor cells,” Nature Cell Biology Published online: 1 Nov. 2004, DOI: 10.1038/ncb1181

13. Jackson K A, Mi T, Goodell M A (1999), “Hematopoietic potential of stem cells isolated from murine skeletal muscle,” Proc Natl Acad Sci USA 96(25):14482-6

14. Brazelton T R, Rossi F M, Keshet G I, Blau H M (2000), “From marrow to brain: expression of neuronal phenotypes in adult mice,” Science 290(5497):1775-9

15. Bjornson C R, Rietze R L, Reynolds B A, Magli M C, Vescovi A L (1999), “Turning brain into blood: a hematopoietic fate adopted by adult neural stem cells in vivo,” Science 283(5401):534-7

16. Slack, J. M. (2000), “Stem cells in epithelial tissues,” Science 287:1431-1433

17. Ferrari G., Cusella-De Angelis G., Coletta M., Paolucci E., Stornaiuolo A., Cossu G., and Mavilio F. (1998), “Muscle regeneration by bone marrow-derived myogenic progenitors,” Science 279:528-30

18. Lagasse E, Connors H, Al-Dhalimy M, Reitsma M, Dohse M, Osborne L, Wang X, Finegold M, Weissman I L, Grompe M (2000), “Purified hematopoietic stem cells can differentiate into hepatocytes in vivo,” Nat Med. 6:1229-34

19. Hirschi, K. K., and Goodell, M. A. (2002), “Hematopoietic, vascular and cardiac fates of bone marrow-derived stem cells,” Gene Ther. 9:648-652

20. Theise N. D. et al. (2000), “Liver from bone marrow in humans,” Hepatology 32:11-16

21. Kleeberger W. et al. (2002), “High frequency of epithelial chimerism in liver transplants demonstrated by microdissection and STR-analysis,” Hepatology 35:110-116

22. Weimann J. M. et al. (2003), “Contribution of transplanted bone marrow cells to Purkinje neurons in human adult brains,” Proc. Natl. Acad. Sci. USA 100:2088-2093

23. Quaini F. et al. (2002), “Chimerism of the transplanted heart,” N. Engl. Med 346:5-15

24. Blau H. M. et al. (2001), “The evolving concept of a stem cell: entity or function?” Cell 105:829-841

25. Goodell M. A. et al. (2001), “Stein cell plasticity in muscle and bone marrow,” Ann. NY Acad. Sci. 938:208-218

26. Krause D. S. (2002), “Plasticity of marrow-derived stem cells,” Gene Ther. 9:754-75 8

27. Wulf G. G. et al. (2001), “Somatic stein cell plasticity,” Exp Hematol. 29:1361-1370

28. Pittenger M. F. et al. (1999), “Multilineage potential of adult human mesenchymal stem cells,” Science 284:143-147

29. Liechty K. W. et al. (2000), “Human mesenchymal stem cells engraft and demonstrate site-specific differentiation after in utero transplantation in sheep,” Nature Med. 6:1282-1286

XIII. Li A. et al. (2003), “IL-8 directly enhanced endothelial cell survival, proliferation, and matrix metalloproteinases production and regulated angiogenesis”, Journal of immunol. 170:3369-3376.

XIV. Laterveer L. et al. (1995), “Interleukin-8 induces rapid mobilization of hematopoietic stem cells with radioprotective capacity and long-term myelolymphoid repopulating ability”, Blood 85:2269-75.

XV. Scho″mig K. et al. (2006), “Interleukin-8 is associated with circulating CD133+ progenitor cells in acute myocardial infarction”, European Heart Journal 27: 1032-1037

30. Sang Y Y, Collector M I, Baylin S B, Diehl A M, Sharkis S J (2004), “Hematopoietic stem cells convert into liver cells within days without fusion,” Nat Cell Biol. 6(6):532-9. Epub May 9, 2004

31. Bittner R. E., Schofer C., Weipoltshammer K., Ivanova S., Streubel B., Hauser E., Freilinger M., Hoger H., Elbe-Burger A., and Wachtler F. (1999), “Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx mice,” Anat. Embryol. (Berl) 199:391-396

32. Mezey E, Chandross K J, Harta G, Maki R A, McKercher S R (2000), “Turning blood into brain: cells bearing neuronal antigens generated in vivo from bone marrow,” Science. 290(5497):1779-82

33. Douglas W. L., Dimmeler S. (2004), “Therapeutic angiogenesis and vasculogenesis for ischemic diseases. Part I: Angiogenic cytokines,” Circulation 109:2487-2491

34. Douglas W. L., Dimmeler S. (2004), “Therapeutic angiogenesis and vasculogenesis for ischemic diseases. Part II: Cell-based therapy,” Circulation 109:2692-2697

35. Rodda S J, Kavanagh S J, Rathjen J, Rathjen P D (2002), “Embryonic stem cell differentiation and the analysis of mammalian development,” Int J Dev Biol. 46(4):449-58

36. Amit M., Carpenter M. K., Inokuma M. S., Chiu C. P., Harris C. P., Waknitz M. A., Itskovitz-Eldor J., and Thomson J. A. (2000), “Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture,” Dev Biol. 227(2):271-8

37. Aoki S, Toda S, Sakemi T, Sugihara H (2003), “Coculture of endothelial cells and mature adipocytes actively promotes immature preadipocyte development in vitro,” Cell Struct Funct. 28(1):55-60

38. Wan H, An Y, Zhang Z, Zhang Y, Wang Z (2003), “Differentiation of rat embryonic neural stem cells promoted by co-cultured Schwann cells,” Chin Med J (Engl). 116(3):428-31

39. Kollet O, Shivtiel S, Chen Y Q. et al. (2003), “HGF, SDF-1, and MMP-9 are involved in stress-induced human CD34+ stem cell recruitment to the liver,” J Clin Invest. 112(2):160-9

40. Badorff C, Brandes R P, Popp R, Rupp S, Urbich C, Aicher A, Fleming I, Busse R, Zeiher A M, Dimmeler S (2003), “Transdifferentiation of blood-derived human adult endothelial progenitor cells into functionally active cardiomyocytes,” Circulation 107(7):1024-32

41. Bianco, P. and Robey P. G. (2001), “Stem cells in tissue engineering,” Nature 414:118-121

42. Lagasse E. et al. (2001), “Toward regenerative medicine,” Immunity 14:425-436

43. Stock U. A., Vacanti J. P. (2001), “Tissue engineering: current state and prospects,” Ann. Rev. Med 52:443-451

44. Kim W. S. et al. (1994), “Bone defect repair with tissue-engineered cartilage,” Plast. Recontr. Surg. 94:580-584

45. Petite H. et al. (2000), “Tissue-engineered bone regeneration,” Nature Biotechnol. 18:959-963

46. Jackson K A, Majka S M, Wang H, Pocius J, Hartley C J, Majesky M W, Entman M L, Michael L H, Hirschi K K, Goodell M A (2001), “Regeneration of ischemic cardiac muscle and vascular endothelium by adult stem cells,” J Clin Invest. 107(11):1395-402

47. Ramiya V. K. et al. (2000), “Reversal of insulin-dependent diabetes using islets generated in vitro from pancreatic stem cells,” Nature Medicine 6:278-282

48. Rafii S., Lyden D. (2003), “Therapeutic stem and progenitor cell transplantation for organ vascularization and regeneration,” Nature Medicine 9:702-712

49. Gussoni E., Soneoka Y., Strickland C., Buzney E., Khan M., Flint A., Kunkel L., and Mulligan R. (1999), “Dystrophin expression in the mdx mouse restored by stem cell transplantation,” Nature 401:390-4

50. Zhao Y et al. (2003), “A human peripheral blood monocyte-derived subset acts as pluripotent stem cells,” Proc. Natl. Acad. Sci. USA 100:2426-2431

51. Kohji N, Masayuki Y, Yasutaka H. et al. (2004), “Corneal reconstruction with tissue-engineered cell sheets composed of autologous oral mucosal epithelium,” N Engl J Med 351:1187-96

52. Kayisli U. A., Luk J, Guzeloglu-Kayisli O. et al. (2005), “Regulation of angiogenic activity of human endometrial endothelial cells in culture by ovarian steroids,” J Clin Endocrinol Metab 89:5794-5802

53. Dimmeler S. (2005), “Circulating endothelial precursors: Identification of functional subpopulations,” Blood 106(7):2231-2232

54. Urbich C. et al. (2004), “Endothelial progenitor cells: Characterization and role in vascular biology,” Circulation Research 95:343-353

A. Asahara T, Murohara T, Sullivan A, et al. (1997), “Isolation of putative progenitor endothelial cells for angiogenesis,” Science 275:964-967.

B. Kalka C, Masuda H, Takahashi T, et al. (2000), “Transplantation of ex vivo expanded endothelial progenitor cells for therapeutic neovascularization,” Proc Natl Acad Sci USA. 97:3422-3427.

C. Assmus B, Schachinger V, Teupe C, et al. (2002), “Transplantation of Progenitor Cells and Regeneration Enhancement in Acute Myocardial Infarction (TOPCARE-AMI),” Circulation. 106:3009-3017.

D. Yoon C. H, Hur J., Park K W, et al. (2005), “Synergistic Neovascularization by Mixed Transplantation of Early Endothelial Progenitor Cells and Late Outgrowth Endothelial Cells,” Circulation. 112:1618-1627.

K DeLisser, H. M., Christofidou-Solomidou, R. M. Strieter, M. D. et al. (1997), “Involvement of endothelial PECAM-1/CD31 in angiogenesis,” Am J Pathol. 151: 671-677.

F. Kawamoto A., Tkebuchava T., Yamaguchi J. I., et al. (2003), “Intramyocardial Transplantation of Autologous Endothelial Progenitor Cells for Therapeutic Neovascularization of Myocardial Ischemia,” Circulation. 107:461-468

G. Newman P. J. (1997), “The Biology of PECAM-1,” J Clin Invest. 99:3-8.

H. Vecchi, A., C. Garlanda, M. G. Lampugnani, M. Resnati, et al. (1994), “Monoclonal antibodies specific for endothelial cells of mouse blood vessels. Their application in the identification of adult and embryonic endothelium,” Eur J Cell Biol. 63: 247-254.

H1. Kanayasu-Toyoda T., Yamaguchi T., Oshizawa T., et al. (2003), “CD31 (PECAM-1)-Bright Cells Derived From AC133-Positive Cells in Human Peripheral Blood as Endothelial-Precursor Cells,” Journal of Cell. Physiol. 195:119-129.

I. Yamamoto K., Takahashi T., Asahara T., et al. (2003), “Proliferation, differentiation, and tube formation by endothelial progenitor cells in response to shear stress,” J Appl Physiol. 95: 2081-2088.

J. Cohen S., and Leor J. (2004), “Rebuilding Broken Hearts,” Scientific American, November: 45-51.

K. US Patent Application Publication 2004/0228897 to Zhang et al.

L. US Patent Application Publication 2005/0272152 to Xu et al.

SUMMARY OF THE INVENTION

In the context of the present patent application and in the claims, a “core cell population” (CCP) is a population of at least 5 million cells which have a density of less than 1.072 g/ml, and at least 1% of which are CD34+CD45−/Dim (i.e., at least 50,000 of the cells are both (a) CD34 positive and (b) CD45 negative or CD45 Dim).

A CCP is typically, but not necessarily, generated from a hematopoietic source.

For most applications, at least 40% of the CCP is CD31Bright (i.e., at least 2 million cells out of the 5 million cells are CD31Bright).

While not being limited to any method of detection, cells expressing increased amounts of CD31 relative to isotype control are termed “CD31Bright” cells, because these cells bear more CD31 molecules relative to other cells, and thus tend to fluoresce brightly when stained with fluorescently-labeled antibodies. In this context, in the specification and in the claims, “bright” means that the fluorescence intensity of the labeled cellular marker of interest is at least 50 times higher (if measured using flow cytometry) than the isotype control intensity.

In accordance with an embodiment of the present invention, a method for producing a progenitor/precursor cell population (PCP) is provided, comprising (a) processing cells extracted from a cell donor to yield a CCP, and (b) stimulating the CCP to differentiate into the progenitor/precursor cell population. In the context of the specification and in the claims, “progenitor/precursor” cells are partially differentiated cells that are able to divide and give rise to differentiated cells.

While for some applications described herein, the density of the cells in the CCP is typically less than 1.072 g/ml (as described), for some applications, the CCP has at least 5 million cells having a density of less than 1.062 g/ml.

In the context of the specification and in the claims, an “elemental cell population” (ECP) is a population of at least 5 million cells which have a density of less than 1.072 g/ml, at least 1.0% of which are CD34+CD45−/Dim, and at least 30% of which are CD31Bright. Typically, but not necessarily, at least 40% of the cells in the ECP are CD31Bright. Typically, but not necessarily, at least 30% of the cells in the ECP are CD14+. Typically, but not necessarily, at least 1.5% or at least 2% of the cells in the ECP are CD34+CD45−/Dim. For some applications, the ECP has at least 5 million cells having a density of less than 1.062 g/ml. It is typically but not necessarily the case that a CCP is also an ECP. It is noted that, although for simplicity, embodiments of the present invention are described herein with respect to procedures relating to a CCP, the scope of the present invention includes, in each instance, performing the same procedure in relation to an ECP.

An “initiating cell population” (ICP), in the context of the specification and in the claims, is a cell population that can differentiate into a PCP. CCPs and ECPs are both examples of an ICP. An ICP is typically but not necessarily created by a process that comprises separating lower density cells (that are included in the ICP) from higher density cells. Such a separation may be accomplished, for example, by use of one or more gradients.

For some applications, the CCP-derived progenitor cells are used as a therapeutic cell product (e.g., for cancer therapy, for tissue regeneration, for tissue engineering, and/or for tissue replacement), as a research tool (e.g., for research of signal transduction, or for screening of growth factors), and/or as a diagnostic tool. When the CCP-derived progenitor cells are used as a therapeutic cell product, they are typically administered to a patient, in whom the progenitor cells mature into the desired cells (e.g., endothelial cells, retinal cells, etc.).

In an embodiment, at least one result of at least one stage in a process described herein is used as a diagnostic indicator. For example, pathology of a patient may be indicated if an in vitro procedure performed on extracted blood of the patient does not produce a CCP, when the same procedure performed on cells extracted from a healthy volunteer would result in production of the CCP. Alternatively or additionally, a pathology of a patient may be indicated if an in vitro stimulation procedure performed on an autologous CCP does not produce a desired number of progenitor cells of a particular class, when the same procedure would produce the desired number of progenitor cells of a particular class from a CCP derived from cells of a healthy volunteer. Further alternatively or additionally, a pathology of a patient may be indicated if one or more in vitro protocols used to assess a PCP do not yield the same results as a PCP originated from a healthy volunteer. Still further alternatively or additionally, a pathology of a patient may be indicated if one or more protocols used to assess a PCP following implantation within a patient do not perform as expected (e.g., like a PCP implanted in a healthy animal or human volunteer, or in an animal model of a similar disease).

When hematopoietic stem cells are used as a source to create the CCP, the resultant CCP is typically but not necessarily characterized by at least 40% of the cells in the CCP being CD31Bright, and at least 2.2% or at least 2.5% of the cells being CD34+CD45−/Dim.

Typically, the process of stimulating the CCP takes between about 2 and about 15 days (e.g., between about 3 and about 15 days), or between about 15 and about 120 days (e.g., between about 15 and about 30 days). Alternatively, stimulating the CCP takes less than 2 days, or more than 120 days.

The mammalian cell donor may be human or non-human, as appropriate. For some applications, the mammalian cell donor ultimately receives an administration of a product derived from the CCP, while for other applications, the mammalian cell donor does not receive such a product. Stem cells that can be used to produce the CCP are typically but not necessarily derived from one or more of the following source tissues: embryonic tissue, umbilical cord blood or tissue, neonatal tissue, adult tissue, bone marrow, mobilized blood, peripheral blood, peripheral blood mononuclear cells, skin cells, and other stem-cell-containing tissue. It is noted that the stem cells may be obtained from fresh samples of these sources or from frozen and then thawed cells from these source tissues.

The CCP is typically prepared by generating or obtaining a single cell suspension from one of the abovementioned source tissues. For example, mobilized blood mononuclear cells may be extracted using a 1.077 g/ml density gradient, e.g., a Ficoll™ gradient, including copolymers of sucrose and epichlorohydrin. It is to be noted that such a gradient is not used for all applications, e.g., for applications in which a single cell suspension is generated from a non-hematopoietic source (e.g., mucosal or skin cells). The output of this gradient is then typically passed through a second gradient (e.g., a Percoll™ gradient, including polyvinylpyrrolidone-coated silica colloids), suitable for selecting cells having a density less than 1.072 g/ml or less than 1.062 g/ml. These selected cells then typically propagate, in vitro, until they become a CCP. As appropriate, other density gradients may be used, independently of or in combination with those cited above in order to enrich the designated cells of the CCP. For example, an OptiPrep™ gradient, including an aqueous solution of Iodixanol, and/or a Nycodenz™ gradient may also be used.

The CCP is typically stimulated to generate progenitor cells of one or more of the following cell classes:

Blood cells (e.g., red blood cells and/or white blood cells (such as T cells or B cells));

Neural lineage cells (e.g., CNS neurons, oligodendrocytes, astrocytes, peripheral nervous system (PNS) neurons, and retinal cells (including, but not limited to, photoreceptors, pigment epithelium cells or retinal ganglion cells).

Endothelial cells;

Pericytes;

Smooth muscle cells;

Cardiomyocytes;

Osteoblasts;

Pancreatic endocrine or exocrine cells (e.g., beta cells or alpha cells);

Hepatic tissue (e.g., hepatocytes); and

Kidney cells.

For some applications, the CCP is transfected with a gene prior to the stimulation of the CCP, whereupon the CCP differentiates into a population of desired progenitor cells containing the transfected gene. Typically, these progenitor cells are then administered to a patient. For some applications, the PCP is transfected with a gene. Typically, these PCP cells are then administered to a patient.

In order to stimulate the CCP to differentiate into a desired class of progenitor cells, or in association with stimulation of the CCP to differentiate into a desired class of progenitor cells, the CCP is typically directly or indirectly co-cultured with “target tissue.” The “target tissue” typically but not necessarily includes tissue from an organ whose cells represent a desired final state of the progenitor cells. For example, the target tissue may include brain or similar tissue, or heart or similar tissue, if it is desired for the progenitor cells to differentiate into brain tissue or into heart tissue, respectively. Other examples include:

(a) co-culturing the CCP with peripheral nerves (and/or culturing the CCP in conditioned medium derived therefrom), to induce differentiation of the CCP into peripheral neurons;

(b) co-culturing the CCP with central nervous system (CNS) nerves (and/or culturing the CCP in conditioned medium derived therefrom), to induce differentiation of the CCP into CNS neurons;

(c) co-culturing the CCP with retinal tissue (and/or culturing the CCP in conditioned medium derived therefrom), to induce differentiation of the CCP into retinal tissue. The retinal tissue may include, for example, one or more of: pigment epithelium, or photoreceptors. As appropriate, the retinal tissue may comprise fetal retinal tissue, embryonic retinal tissue, or mature retinal tissue;

(d) co-culturing the CCP with blood vessel tissue (and/or culturing the CCP in conditioned medium derived therefrom), to induce differentiation of the CCP into angiogenic lineage tissue and/or cardiomyocytes (CMCs);

(e) co-culturing the CCP with cardiac tissue (and/or culturing the CCP in conditioned medium derived therefrom), to induce differentiation of the CCP into CMCs;

(f) co-culturing the CCP with pancreatic endocrine or exocrine tissue (and/or culturing the CCP in conditioned medium derived therefrom), to induce differentiation of the CCP into pancreatic endocrine or exocrine cells; and

(g) co-culturing the CCP with smooth muscle tissue (and/or culturing the CCP in conditioned medium derived therefrom), to induce differentiation of the CCP into smooth muscle cells.

Techniques described herein with respect to use of a target tissue may be used with any “sample” tissue, regardless of whether it is desired for the CCP to differentiate into a PCP having cells like those in the sample tissue.

For some applications, slices or a homogenate of the target tissue are used for co-culturing, although other techniques for preparing the target tissue will be apparent to a person of ordinary skill in the art who has read the disclosure of the present patent application.

The target tissue may be in essentially direct contact with the CCP, or separated therefrom by a semi-permeable membrane. As appropriate, the target tissue may be autologous, syngeneic, allogeneic, or xenogeneic with respect to the source tissue from which the CCP was produced. Alternatively or additionally, the CCP is cultured in a conditioned medium made using target, tissue (e.g., a target tissue described hereinabove), that is autologous, syngeneic, allogeneic, or xenogeneic with respect to the source tissue from which the CCP was produced. For some applications, the target tissue and the CCP are co-cultured in the conditioned medium. It is to be noted that the source of the target tissue may also be tissue from a cadaver, and/or may be lyophilized, fresh, or frozen.

Alternatively or additionally, for some applications, to produce a desired class of progenitor cells, cells from the CCP are cultured in the presence of stimulation caused by “stimulation factors,” e.g., one or more antibodies, cytokines, growth factors, tissue-derived extra cellular matrix, and/or other molecules, such as: IL-8, anti-IL-8, anti-CD34, anti-Tie-2, anti-CD133, anti-CD117, LIF, EPO, IGF, b-FGF, M-CSF, GM-CSF, TGF alpha, TGF beta, VEGF, BHA, BDNF, NGF, NT3, NT4/5, GDNF, S-100, CNTF, EGF, NGF3, CFN, ADMIF, estrogen, cortisone, dexamethasone, or any other molecule from the steroid family, prolactin, an adrenocorticoid hormone, ACTH, glutamate, serotonin, acetylcholine, NO, retinoic acid (RA), heparin, insulin, forskolin, a statin, an anti-diabetic drug (e.g., a thiazolidinedione such as rosiglitazone), NO, MCDB-201, MCT-165, glatiramer acetate (L-glutamic acid, L-alanine, L-tyrosine, L-lysine), a glatiramer acetate-like molecule, IFN alpha, IFN beta, or any other immunoregulatory agent, sodium selenite, linoleic acid, ascorbic acid, transferrin, 5-azacytidine, PDGF, VEGF, cardiotrophin, and thrombin.

In the context of the specification and in the claims, a “glatiramer acetate-like molecule” means a copolymer comprising:

(a) the same four amino acids as in glatiramer acetate, but in different ratios, (e.g., within 5%, 10%, or 25% of their current values of L-glutamic acid:L-alanine:L-tyrosine:L-lysine=0.141:0.427:0.095:0.338);

(b) three of the four amino acids in glatiramer acetate, but the fourth amino acid is replaced by a different naturally-occurring or synthetic amino acid;

(c) four amino acids, in which at least one of the amino acids is an enantiomer of the corresponding amino acid in glatiramer acetate, and the remainder of the amino acids (if any) are the corresponding L-amino acids that are in glatiramer acetate; or

(d) a combination one or more of (a), (b), and (c).

It is to be appreciated that the particular stimulation factors described herein are by way of illustration and not limitation, and the scope of the present invention includes the use of other stimulation factors. As appropriate, these may be utilized in a concentration of between about 100 pg/ml and about 100 μg/ml (or molar equivalents). Typically, particular stimulation factors are selected in accordance with the particular class of progenitor cells desired. For example, to induce neural progenitor cells, one or more of the following stimulation factors are used: BHA, BDNF, NGF, NT3, NT4/5, GDNF, MCT-165, glatiramer acetate, a glatiramer acetate-like molecule, IFN alpha, IFN beta or any other immunoregulatory agent, S-100, CNTF, EGF, NGF3, CFN, ADMIF, and acetylcholine. In another example, to induce CMC progenitors, one or more of the following stimulation factors are used: bFGF, cortisone, estrogen, progesterone, or any other molecule form the steroid family, NO, sodium selenite, linoleic acid, ascorbic acid, retinoic acid (RA) or any other derivative of vitamin D, transferrin, 5-azacytidine, MCT-165, glatiramer acetate, a glatiramer acetate-like molecule, IFN alpha, IFN beta, or any other immunoregulatory agent, TGF-beta, insulin, EGF, IGF, PDGF, VEGF, cardiotrophin, MCDB201, and thrombin.

For some applications, the stimulation factors are introduced to the CCP in a soluble form, and/or in an aggregated form, and/or attached to a surface of a culture dish. In an embodiment, the CCP is incubated on a surface comprising a growth-enhancing molecule other than collagen or fibronectin. The growth-enhancing molecule may comprise, for example, VEGF or another suitable antibody or factor described herein. As appropriate, the growth-enhancing molecule may be mixed with collagen or fibronectin or plasma, or may be coated on the surface in a layer separate from a layer on the surface that comprises collagen or fibronectin or plasma. Alternatively, the only growth-enhancing molecule(s) on the surface of the culture dish is collagen and/or fibronectin and/or plasma.

In the context of the present patent application and in the claims, a surface “comprising” or “including” a molecule means that the molecule is coated on the surface, attached to the surface, or otherwise integrated into the surface.

Following stimulation of the CCP, the resultant product is typically tested to verify that it has differentiated into a desired form. Characterization of the differentiated cells is performed according to the cells' phenotypical, genotypical and physiological features. In accordance with an embodiment of the present invention, the cells are characterized by assessing functional/physiological activity thereof, in combination with or in place of evaluating the presence or absence of certain cellular markers. Evaluating functional/physiological activity of the cells following the stimulation of the CCP helps increase the likelihood that the product obtained and designated for in vivo use will perform as expected.

For example, when angiogenic cell precursors (ACPs) (which also include endothelial progenitor cells (EPCs)) are the desired product, the product is typically positive for the generation and/or expression of one or more of CD34, CD 117, CD133, Tie-2, CD31, CD34+CD133+, KDR, CD34+KDR+, CD144, von Willebrand Factor, SH2 (CD105), SH3, fibronectin, collagen (types I, III and/or IV), ICAM (type 1 or 2), VCAM1, Vimentin, BMP-R IA, BMP-RII, CD44, integrin b1, aSM-actin, and MUC18, CXCR4. Additionally, the ACP product typically functionally demonstrates uptake of Acetylated-Low Density Lipoprotein (Ac-LDL) (i.e., the product is Ac-LDL+) and/or secretes one or more of the following molecules: Interleukin-8 (IL-8), VEGF, Angiogenin, Matrix metalloproteinase 2 (MMP-2), or Matrix metalloproteinase 9 (MMP-9). Alternatively or additionally, the ACP product generates tube-like structures on a semi-solid matrix, and/or migrates towards chemoattractants (such as SDF-1 or VEGF), and/or proliferates in response to cell activation, and/or generates typical cell colonies/clusters. For some applications, in order to further characterize the cells, CD31Bright cells that demonstrate uptake of Ac-LDL are examined.

Typically, greater than 1.5% of the core cell population that was stimulated demonstrates one or more of the abovementioned characteristics. Alternatively, if neural progenitor cells are the desired product, then the product is typically positive for the generation and/or the expression of one or more of: Nestin, NSE, Notch, numb, Musashi-1, presenilin, FGFR4, Fz9, SOX 2, CD133, CD15, GD2, rhodopsin, recoverin, calretinin, PAX6, RX, Chx10, O4, and GFAP. Further alternatively, if cardiomyocyte (CMC) progenitors are the desired product, then the product is typically positive for the generation and/or the expression of one or more of: CD31, CD117, sarcomeric alpha-actin, beta-actin, alpha-actinin, desmin, cardiac troponin T, connexin43, alpha/beta-MHC, sarcomeric alpha-tropomyosin, Troponin I, GATA-4, Nkx2.5/Csx,and MEF-2.

For some applications, the time duration between collecting cells from the cell donor and using the CCP-derived progenitor cells (e.g., for administration into a patient), is reduced in order to effect almost immediate use thereof. Alternatively, the cells are preserved at one or more points in the process. For example, the CCP may be frozen prior to the stimulation thereof that generates progenitor cells. Alternatively, the CCP is stimulated in order to generate desired progenitor cells, and these progenitor cells are frozen. In either of these cases, the frozen cells may be stored and/or transported, for subsequent thawing and use. “Transport,” in the context of the specification and the claims, means transport to a remote site, e.g., a site greater than 10 km or 100 km away from a site where the CCP is first created.

It is noted that certain applications are suitable for large-scale commercialization, including freezing and transport, such as (a) generation of stores of CCPs, (b) generation of stores of PCPs, (such as hematopoietic stem cells able to mature into CMCs), and (c) stem cell banks where individuals may store a CCP or differentiated progenitor cells, for possible later use. Other applications (such as acute post-stroke autologous administration of neuronal stem cells) may not benefit, or may not benefit as greatly, from the time delays provided by freezing of cells, although the technique may be useful for some purposes.

For some applications, the CCP is cultured for a period lasting between about 1 and about 20 days (e.g., between about 1 and 5 days) in a culture medium comprising less than about 5% serum. Alternatively, the CCP is cultured for a period lasting between about 1 and about 20 days (e.g., between about 1 and about 5 days) in a culture medium comprising greater than about 10% serum. In an embodiment, one of these periods follows the other of these periods.

For some applications, the CCP is cultured, during a low-serum time period, in a culture medium comprising less than about 10% serum, and, during a high-serum time period, in a culture medium comprising greater than or equal to about 10% serum. In an embodiment, culturing the CCP during the low-serum time period comprises culturing the CCP for a duration of between about 1 and about 20 days (e.g., between about 1 and about 5 days). Alternatively or additionally, culturing the CCP during the high-serum time period comprises culturing the CCP for a duration of between about 1 and about 120 days (e.g., between about 1 and about 30 days). Typically, culturing the CCP during the low-serum time period is performed prior to culturing the CCP during the high-serum time period. Alternatively, culturing the CCP during the low-serum time period is performed following culturing the CCP during the high-serum time period.

For some applications, during a hypoxic time period lasting at least about 2 hours, the CCP is cultured under hypoxic conditions, and, during a non-hypoxic time period lasting at least about 1 day, the CCP is cultured under non-hypoxic conditions. Culturing the CCP under hypoxic conditions may be performed prior to or following culturing the CCP under non-hypoxic conditions. Typically, but not necessarily, the hypoxic and non-hypoxic time-periods are within a culturing time period lasting less than about 120 days (e.g., less than about 30 days), and culturing the CCP under hypoxic conditions comprises culturing the CCP under hypoxic conditions during the first about two days of the culturing time period. Alternatively or additionally, culturing the CCP under hypoxic conditions comprises culturing the CCP under hypoxic conditions during the last about two days of the culturing time period. Further alternatively or additionally, culturing the CCP under hypoxic conditions comprises culturing the CCP under hypoxic conditions for at least about 2 hours between a first two days and a last two days of the culturing time period.

For some applications, the CCP is cultured in a culture medium comprising at least one of the following: erythropoietin, a statin, and an antidiabetic agent (e.g., a thiazolidinedione such as rosiglitazone). Alternatively or additionally, the CCP is cultured in the presence of one or more proliferation-differentiation-enhancing agents, such as, anti-CD34, anti-Tie-2, anti-CD133, anti-CD117, LIF, EPO, IGF, b-FGF, M-CSF, GM-CSF, TGF alpha, TGF beta, VEGF, BHA, BDNF, NGF, NT3, NT4/5, GDNF, S-100, CNTF, EGF, NGF3, CFN, ADMIF, estrogen, prolactin, an adrenocorticoid hormone, ACTH, glutamate, serotonin, acetylcholine, NO, retinoic acid (RA) or any other vitamin D derivative, heparin, insulin, forskolin, cortisone, cortisol, dexamethasone, progesterone, or any other molecule from the steroid family, a statin, or an anti-diabetic drug (e.g., a thiazolidinedione such as rosiglitazone), MCDB-201, MCT-165, glatiramer acetate, a glatiramer acetate-like molecule, IFN alpha, IFN beta or any other immunoregulatory agent, sodium selenite, linoleic acid, ascorbic acid, transferrin, 5-azacytidine, PDGF, VEGF, cardiotrophin, and thrombin.

In an embodiment, techniques described herein are practiced in combination with (a) techniques described in one or more of the references cited herein, (b) techniques described in U.S. Provisional Patent Application 60/576,266, filed Jun. 1, 2004, (c) techniques described in U.S. Provisional Patent Application 60/588,520, filed Jul. 15, 2004, (d) techniques described in U.S. Provisional Patent Application 60/668,739, filed Apr. 5, 2005, (e) techniques described in U.S. Provisional Patent Application 60/636,391, filed Dec. 14, 2004, (f) techniques described in PCT Patent Application PCT/IL2005/001345, filed Dec. 14, 2005, and/or PCT Patent Application PCT/IL2005/001348, filed Dec. 14, 2005. Each of these patent applications is assigned to the assignee of the present patent application and is incorporated herein by reference, and the scope of the present invention includes embodiments described therein.

In an embodiment, a method is provided comprising culturing the CCP in a first container during a first portion of a culturing period; removing all or at least some cells of the CCP from the first container at the end of the first portion of the period; and culturing, in a second container during a second portion of the period, the cells removed from the first container. For example, removing at least some of the CCP cells may comprise selecting for removal cells that adhere to a surface of the first container.

When the cells from a progenitor/precursor cell population (PCP) derived from a CCP are designated for implantation into a human, they should be generally free from any bacterial or viral contamination. Additionally, in the case of a PCP of angiogenic cell precursors (ACPs), one or more of the following phenotypical, genotypical and physiological conditions should typically be met:

(I) Cells should be morphologically characterized as (a) larger in size than 20 uM and/or (b) elongated, spindle-shaped or irregular-shaped and/or (c) granulated or dark nucleated and/or (d) with flagella-like structures or pseudopodia and/or (e) fibroblast-like or polygonal in shape.

(II) Final cell suspension should typically contain at least 1 million cells expressing one or more of the following markers: CD31Bright, CD34, CD117, CD133, Tie-2, CD34+CD133+, KDR, CD34+KDR+, CD144, von Willebrand Factor, SH2 (CD105), SH3, fibronectin, collagen (types I, III and/or IV), ICAM (type 1 or 2), VCAM1, Vimentin, BMP-R IA, BMP-RII, CD44, integrin b1, aSM-actin, and MUC18, CXCR4

(III) Cells should be able to uptake Ac-LDL.

(IV) Cells expressing CD31Bright should also demonstrate the ability to uptake Ac-LDL (e.g., at least about 10% or about 25% of cells that are CD31Bright also are able to uptake Ac-LDL).

(V) Cells should generally secrete one or more of the following molecules: IL-8, Angiogenin, VEGF, MMP2, and MMP9.

(VI) Cells should generally form tube-like structures when cultured on a semi-solid matrix containing growth factors.

(VII) Cells should generally migrate chemotactically towards different chemoattractants, such as SDF-1 and VEGF.

(VIII) Cells should generally form typical colonies and/or clusters when cultured in medium supplemented with growth factors such as VEGF and GM-SCF.

It is noted that the cells in CCPs generated from various tissues typically can be characterized as having greater than 75% viability.

It is noted that CCPs generated from blood, bone marrow, and umbilical cord blood, typically have greater than 70% of their cells being CD45+.

In some embodiments of the present invention, a novel composition of matter is provided, comprising (a) a cell population, or (b) a mixture comprising a cell population and molecules produced by the cell population, wherein (a) or (b) are produced by a method described herein (for example, in one of the methods set forth in the following paragraphs preceding the Brief Description section of the present patent application, or in one of the methods described in the Detailed Description section of the present patent application).

There is therefore provided, in accordance with an embodiment of the invention, a composition of matter, including a population of cultured cells that includes a sub-population of cells that both stain as CD31Bright and demonstrate uptake of Ac-LDL+.

In an embodiment, the sub-population includes at least 10%, 25%, or 50% of the cells in the population.

In an embodiment, at least 1.5% of the cells of the population include at least one morphological feature selected from the group consisting of: a cell size larger than 20 um, an elongated cell, a spindle-shaped cell, an irregularly-shaped cell, a granulated cell, a cell including an enlarged dark nucleus, a multinuclear cell, a cell including flagella-like structures, a cell including pseudopodia, and a cell having a polygonal shape.

In an embodiment, at least 1.5% of the cells of the population include at least one feature selected from the group consisting of: CD34, CD117, CD133, Tie-2, CD34+CD133+, KDR, CD34+KDR+, CD144, von Willebrand Factor, SH2 (CD105), SH3, fibronectin, collagen type I, collagen type III, collagen type IV, ICAM type 1, ICAM type 2, VCAM1, vimentin, BMP-R IA, BMP-RII, CD44, integrin b1, aSM-actin, MUC18, and CXCR4.

In an embodiment, at least 1.5% of the cells of the population secrete at least one molecule selected from the group consisting of: IL-8, angiogenin, VEGF, MMP2, and MMP9.

In an embodiment, at least 1.5% of the cells of the population include at least one feature selected from the group consisting of: a tube-like structure, a tendency to form a colony, a tendency to form a cluster, and a tendency to migrate towards a chemoattractant.

There is further provided, in accordance with an embodiment of the invention, a method including in vitro stimulating an initiating cell population (ICP) of at least 5 million cells that have a density of less than 1.072 g/ml, at least 1% of which are CD34+CD45−/Dim, and at least 25% of which are CD31Bright, to differentiate into a progenitor/precursor cell population (PCP).

There is still further provided, in accordance with an embodiment of the invention, a method including in vitro stimulating an initiating cell population (ICP) of at least ten thousand cells that have a density of less than 1.072 g/ml and at least 25% of which are CD31Bright to differentiate into a progenitor/precursor cell population (PCP).

There is yet further provided, in accordance with an embodiment of the invention, a method including separating lower density cells from higher density cells, the lower density cells defining an initiating cell population (ICP) at least 40% of which are CD31Bright, and in vitro stimulating the ICP to differentiate into a progenitor/precursor cell population (PCP).

In an embodiment, stimulating the ICP includes culturing the ICP for a period lasting between 1 and 5 days in a culture medium including less than or equal to 10% serum.

In an embodiment, stimulating the ICP includes culturing the ICP for a period lasting between 1 and 5 days in a culture medium including less than or equal to 5% serum.

In an embodiment, stimulating the ICP includes culturing the ICP for a period lasting between 1 and 5 days in a culture medium including 5-10% serum.

In an embodiment, stimulating the ICP includes culturing the ICP for a period lasting between 1 and 5 days in a culture medium including less than or equal to 5% serum.

In an embodiment, stimulating the ICP includes culturing the ICP for a period lasting between 1 and 5 days in a culture medium including at least 10% serum.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including a factor selected from the group consisting of: anti-Tie-2, anti-CD133, and anti-CD 117.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including a factor selected from the group consisting of: anti-Tie-2, anti-CD133, and anti-CD117, anti-IL-8, anti IL-8 receptor, IL-8-antagonist, VEGF, anti-VEGF, and anti-VEGF receptor.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including IL-8.

In an embodiment, stimulating the ICP includes culturing the ICP in the presence of a factor selected from the group consisting of: anti IL-8 receptor, IL-8-antagonist, VEGF, anti-VEGF, and anti-VEGF receptor.

In an embodiment, stimulating the ICP includes culturing the ICP in the presence of IL-8.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an identification in the PCP of CXCR8.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells of the PCP include CXCR8.

In an embodiment, characterizing the PCP includes culturing a portion of the PCP on a semi-solid extracellular matrix (ECM), and identifying in the cultured portion a feature selected from the group consisting of: a tube-like structure, a colony, a cluster, and a tendency to migrate towards a chemoattractant.

In an embodiment, characterizing the PCP includes culturing at least a portion of the PCP on a membrane, and identifying a tendency of the at least a portion of the PCP to migrate toward IL-8.

In an embodiment, the ICP includes at least 5 million cells, and stimulating the ICP includes stimulating the ICP that includes the at least 5 million cells.

In an embodiment, at least 1.5% of the cells of the ICP are CD34+CD45−/Dim, and stimulating the ICP includes stimulating the ICP of which at least 1.5% of the cells are CD34+CD45−/Dim.

In an embodiment, at least 2% of the cells of the ICP are CD34+CD45−/Dim, and stimulating the ICP includes stimulating the ICP of which at least 2% of the cells are CD34+CD45−/Dim.

In an embodiment, at least 30% of the cells of the ICP are CD31Bright, and stimulating the ICP includes stimulating the ICP of which at least 30% of the cells are CD31Bright.

In an embodiment, the ICP includes at least 5 million cells that have a density of less than 1.062 g/ml, at least 1% of which are CD34+CD45−/Dim, and stimulating the ICP includes stimulating the ICP that has the at least 5 million cells that have a density of less than 1.062 g/ml.

In an embodiment, at least 50% of cells in the ICP are CD31Bright, and stimulating the ICP includes stimulating the ICP of which at least 50% of cells therein are CD31Bright.

In an embodiment, the method includes preparing the PCP as a product for administration to a patient. Alternatively or additionally, the method includes preparing the PCP as a research tool.

In an embodiment, stimulating the ICP includes only stimulating the ICP if the ICP is derived from a mammalian donor.

In an embodiment, the method includes applying cells extracted from a mammalian donor to one or more gradients suitable for selecting cells having a density less than 1.072 g/ml, and deriving the ICP from the cells applied to the gradient.

In an embodiment, the ICP is characterized by at least 2.5% of the ICP being CD34+CD45−/Dim, and stimulating the ICP includes stimulating the ICP having the at least 2.5% of the ICP that are CD34+CD45−/Dim.

In an embodiment, the ICP is characterized by at least 40% of the ICP being CD31Bright, and stimulating the ICP includes stimulating the ICP having the at least 40% of the ICP that are CD31Bright.

In an embodiment, stimulating the ICP includes stimulating the ICP to differentiate into a pre-designated, desired class of progenitor cells.

In an embodiment, the method includes deriving the ICP from at least one source selected from the group consisting of embryonic tissue, fetal tissue, umbilical cord blood, umbilical cord tissue, neonatal tissue, adult tissue, bone marrow, mobilized blood, peripheral blood, peripheral blood mononuclear cells, skin cells, and plant tissue.

In an embodiment, the method includes deriving the ICP from at least one source selected from the group consisting of: fresh tissue and frozen tissue.

In an embodiment, the method includes identifying an intended recipient of the PCP, and deriving the ICP from at least one source selected from the group consisting of tissue autologous to tissue of the intended recipient, tissue syngeneic to tissue of the intended recipient, tissue allogeneic to tissue of the intended recipient, and tissue xenogeneic to tissue of the intended recipient.

In an embodiment, stimulating the ICP includes culturing the ICP for a period lasting between 1 and 5 days in a culture medium including less than 5% serum.

In an embodiment, stimulating the ICP includes culturing the ICP for a period lasting between 1 and 5 days in a culture medium including at least 10% serum.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including a factor selected from the group consisting of: erythropoietin, a statin, and an antidiabetic agent.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including a factor selected from the group consisting of: estrogen, prolactin, progestin, an adrenocorticoid hormone, ACTH, and cortisone.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including a factor selected from the group consisting of: anti-Tie-2, anti-CD133, and anti-CD117.

In an embodiment, stimulating the ICP includes culturing the ICP in the presence of a factor selected from the group consisting of: erythropoietin, a statin, an antidiabetic agent, a thiazolidinedione, rosiglitazone, a proliferation-differentiation-enhancing agent, anti-CD34, anti-Tie-2, anti-CD133, anti-CD117, LIF, EPO, IGF, b-FGF, M-CSF, GM-CSF, TGF alpha, TGF beta, VEGF, BHA, BDNF, GDNF, NGF, NT3, NT4/5, S-100, CNTF, EGF, NGF3, CFN, ADMIF, estrogen, prolactin, an adrenocorticoid hormone, ACTH, MCT-165, glatiramer acetate, a glatiramer acetate-like molecule, IFN alpha, IFN beta, glutamate, serotonin, acetylcholine, NO, retinoic acid (RA), heparin, insulin, cortisone, and forskolin.

In an embodiment, the method includes preparing the ICP, and facilitating a diagnosis responsive to a characteristic of the preparation of the ICP.

In an embodiment, the method includes freezing the ICP prior to stimulating the ICP.

In an embodiment, the method includes freezing the PCP.

In an embodiment, the method includes transporting the ICP to a site at least 10 km from a site where the ICP is first created, and stimulating the ICP at the remote site.

In an embodiment, the method includes transporting the PCP to a site at least 10 km from a site where the PCP is first created.

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million PCP cells.

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that at least 1.5% of cells of the PCP demonstrate a feature selected from the group consisting of: a desired morphology, a desired cellular marker, a desired cellular component, a desired enzyme, a desired receptor, a desired genotypic feature, and a desired physiological feature.

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million angiogenic cell precursors (ACPs).

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million cardiomyocyte progenitors.

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million neural cell progenitors.

In an embodiment, the method includes transfecting into the PCP a gene identified as suitable for gene therapy.

In an embodiment, the method includes transfecting a gene into the PCP, and subsequently assessing a level of expression of the gene.

In an embodiment, the method includes transfecting a gene into the ICP, and subsequently assessing a level of expression of the gene.

In an embodiment, stimulating the ICP includes culturing the ICP during a period of between 2 and 120 days.

In an embodiment, stimulating the ICP includes culturing the ICP during a period of between 3 and 60 days.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including less than 10% serum, for a duration of between 1 and 120 days.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including at least 10% serum, for a duration of between 1 and 120 days.

In an embodiment, the method includes characterizing the PCP as including angiogenic cell precursors (ACPs), in response to an evaluation of at least a feature selected from the group consisting of: a phenotypical feature of cells in the PCP, a genotypical feature of cells in the PCP, and a physiological feature of cells in the PCP.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an evaluation of at least two of the features.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an evaluation of each of the features.

In an embodiment:

the phenotypical feature includes a morphological feature selected from the group consisting of: a cell size larger than 20 μm, an elongated cell, a spindle-shaped cell, an irregularly-shaped cell, a granulated cell, a cell including an enlarged dark nucleus, a multinuclear cell, a cell including flagella-like structures, a cell including pseudopodia, and a cell having a polygonal shape; and

characterizing the PCP includes characterizing the PCP in response to an evaluation of the selected morphological feature.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells of the PCP have the selected feature.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an identification in the PCP of a feature selected from the group consisting of: CD31, CD31Bright, CD34, CD117, CD133, Tie-2, CD34+CD133+, KDR, CD34+KDR+, CD144, von Willebrand Factor, SH2 (CD105), SH3, fibronectin, collagen type I, collagen type III, collagen type IV, ICAM type 1, ICAM type 2, VCAM1, vimentin, BMP-R IA, BMP-RII, CD44, integrin b1, aSM-actin, MUC18, and CXCR4.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells of the PCP have the selected feature.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an assessment of uptake by the PCP of Ac-LDL.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells of the PCP demonstrate uptake of Ac-LDL.

In an embodiment, the PCP includes CD31Bright PCP cells, and characterizing the PCP includes identifying that at least 10% of the CD31Bright PCP cells demonstrate uptake of Ac-LDL.

In an embodiment, characterizing the PCP includes assessing secretion by the PCP of a molecule selected from the group consisting of: IL-8, angiogenin, VEGF, MMP2, and MMP9.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells of the PCP secrete the selected molecule.

In an embodiment, characterizing the PCP includes culturing a portion of the PCP on a semi-solid extracellular matrix (ECM), and identifying in the cultured portion a feature selected from the group consisting of: a tube-like structure, a colony, a cluster, and a tendency to migrate towards a chemoattractant.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells in the cultured portion have a property selected from the group consisting of: formation of a tube-like structure, an ability to form a colony, a cluster, and a tendency to migrate towards a chemoattractant.

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million ACPs.

In an embodiment, the method includes characterizing the PCP as including a cardiomyocyte (CMC) PCP in response to an evaluation of a feature selected from the group consisting of: a phenotypic feature of cells in the PCP, a genotypic feature on the cells in the PCP, and a physiological feature of cells in the PCP.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an evaluation of at least two of the features.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an evaluation of each of the features.

In an embodiment, the phenotypic feature includes a morphological feature selected from the group consisting of: a cell size larger than 20 um, an elongated cell, an irregularly-shaped cell, a granulated cell, a cell including an enlarged dark nucleus, a multinuclear cell, a cell with dark cytoplasm, and cells arranged in parallel to each other; and

characterizing the PCP includes characterizing the PCP in response to an evaluation of the selected morphological feature.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an identification in the PCP of a feature selected from the group consisting of: CD31, CD117, sarcomeric alpha-actin, beta-actin, alpha-actinin, desmin, cardiac troponin T, Connexin-43, alpha/beta-MHC, sarcomeric alpha-tropomyosin, Troponin I, GATA-4, Nkx2.5/Csx, MLC-2, and MEF-2.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an identification of the PCP. as expressing a gene for a factor selected from the group consisting of: sarcomeric alpha-actin, beta-actin, alpha-actinin, desmin, cardiac troponin T, Connexin-43, alpha/beta-MHC, sarcomeric alpha-tropomyosin, Troponin I, GATA-4, Nkx2.5/Csx, MLC-2 and MEF-2.

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million CMC progenitors.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells of the PCP have a characteristic selected from the group consisting of a CMC-progenitor morphological characteristic, expression of a CMC-associated cellular marker, expression of a CMC-progenitor gene product, and expression of a CMC-progenitor physiological feature.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an identification in the PCP of an action in response to activation of the PCP, the action selected from the group consisting of: increasing intracellular Ca2⁺ level, generating membranal electrophysiological action potentials, and mechanical cellular contraction in vitro.

In an embodiment, activating the PCP to produce the selected action, using a technique selected from the group consisting of: electrical activation of the PCP, and chemical activation of the PCP.

In an embodiment, the method includes:

assessing a phenotypic aspect of the PCP and a genotypic aspect of the PCP and a physiological aspect of the PCP; and

designating the PCP as being suitable for implantation in a patient in response to each of the assessments.

In an embodiment, assessing the phenotypic aspect of the PCP includes assessing an aspect of the PCP selected from the group consisting of: morphology of the PCP, a cellular marker of cells of the PCP, an enzyme of the PCP, a coenzyme of the PCP, and presence of a designated cellular receptor on cells of the PCP.

In an embodiment, assessing the genotypic aspect of the PCP includes assessing an aspect of the PCP selected from the group consisting of: production of a gene by cells of the PCP, expression of a gene by cells of the PCP, and generation of a gene product by cells of the PCP.

In an embodiment, assessing the physiological aspect of the PCP includes assessing an aspect of the PCP selected from the group consisting of: secretion of soluble molecules by cells of the PCP, generation of signals by cells of the PCP, response by cells of the PCP to signals, and an enzymatic reaction performed by cells of the PCP.

In an embodiment, the method includes facilitating a diagnosis responsive to stimulating the ICP to differentiate into the PCP.

In an embodiment, facilitating the diagnosis includes assessing an extent to which the stimulation of the TCP produces a particular characteristic of the PCP.

In an embodiment, the method includes transfecting a gene into the ICP prior to stimulating the ICP.

In an embodiment, transfecting the gene includes transfecting into the ICP a gene identified as suitable for gene therapy.

In an embodiment, the method includes preparing, as a product for administration to a patient, the PCP generated by differentiation of the ICP into which the gene has been transfected.

In an embodiment, stimulating the ICP includes incubating the ICP in a container having a surface including a growth-enhancing factor.

In an embodiment, the growth-enhancing factor is selected from the group consisting of: collagen, plasma, fibronectin, a growth factor, tissue-derived extra cellular matrix, and an antibody to a stem cell surface receptor.

In an embodiment, stimulating the ICP includes incubating the TCP in a container with a surface including a growth-enhancing molecule other than collagen or fibronectin.

In an embodiment, incubating the ICP includes incubating the ICP in a container having a surface that includes, in addition to the growth-enhancing molecule, at least one of: collagen and fibronectin.

In an embodiment, the method includes mixing the growth-enhancing molecule with the at least one of: collagen and fibronectin.

In an embodiment, the method includes applying to the surface a layer that includes the growth-enhancing molecule and a separate layer that includes the at least one of: collagen and fibronectin.

In an embodiment, stimulating the ICP includes:

during a low-serum time period, culturing the ICP in a culture medium including less than 10% serum; and

during a high-serum time period, culturing the ICP in a culture medium including greater than or equal to 10% serum.

In an embodiment, culturing the ICP during the low-serum time period includes culturing the ICP for a duration of between 1 and 60 days.

In an embodiment, culturing the ICP during the low-serum time period includes culturing the ICP for a duration of between 1 and 5 days.

In an embodiment, culturing the ICP during the high-serum time period includes culturing the ICP for a duration of between 1 and 120 days.

In an embodiment, culturing the ICP during the high-serum time period includes culturing the ICP for a duration of between 1 and 60 days.

In an embodiment, culturing the ICP during the low-serum time period is performed prior to culturing the ICP during the high-serum time period.

In an embodiment, culturing the ICP during the low-serum time period is performed following culturing the ICP during the high-serum time period.

In an embodiment, the method includes:

during a hypoxic time period lasting at least 2 hours, culturing the ICP under hypoxic conditions; and

during a non-hypoxic time period lasting at least 1 day, culturing the ICP under non-hypoxic conditions.

In an embodiment, the hypoxic and non-hypoxic time-periods are within a culturing time period lasting less than 30 days, and culturing the ICP under hypoxic conditions includes culturing the cells under hypoxic conditions during a first two days of the culturing time period.

In an embodiment, the hypoxic and non-hypoxic time-periods are within a culturing time period lasting less than 30 days, and culturing the ICP under hypoxic conditions includes culturing the ICP under hypoxic conditions during a last two days of the culturing time period.

In an embodiment, the hypoxic and non-hypoxic time-periods are within a culturing time period lasting less than 30 days, and culturing the ICP under hypoxic conditions includes culturing the ICP under hypoxic conditions for at least 2 hours between a first two days and a last two days of the culturing time period.

In an embodiment, culturing the ICP under hypoxic conditions is performed prior to culturing the ICP under non-hypoxic conditions.

In an embodiment, culturing the ICP under hypoxic conditions is performed following culturing the ICP under non-hypoxic conditions.

In an embodiment, stimulating the ICP includes:

culturing the ICP in a first container during a first portion of a culturing period;

removing at least some cells of the ICP from the first container at the end of the first portion of the period; and

culturing, in a second container during a second portion of the period, the cells removed from the first container.

In an embodiment, the method includes subsequently to the step of culturing in the second container:

culturing the ICP in a primary container during a first portion of an additional culturing period;

removing at least some cells of the ICP from the primary container at the end of the first portion of the additional period; and

culturing, in a secondary container during a second portion of the additional period, the cells removed from the primary container.

In an embodiment, stimulating the ICP includes:

culturing the ICP in a first container during a first portion of a culturing period;

removing cells of the ICP from the first container at the end of the first portion of the period; and

culturing, in a second container during a second portion of the period, the cells removed from the first container.

In an embodiment, removing at least some cells of the ICP includes selecting for removal cells that adhere to a surface of the first container.

In an embodiment, removing at least some cells of the ICP includes selecting for removal cells that do not adhere to a surface of the first container.

In an embodiment, the first container includes on a surface thereof a growth-enhancing molecule, and culturing the ICP in the first container includes culturing the ICP in the first container that includes the growth-enhancing molecule.

In an embodiment, the growth-enhancing molecule is selected from the group consisting of: collagen, plasma, fibronectin, a growth factor, tissue-derived extra cellular matrix and an antibody to a stem cell surface receptor.

In an embodiment, the second container includes on a surface thereof a growth-enhancing molecule, and culturing the ICP in the second container includes culturing the ICP in the second container that includes the growth-enhancing molecule.

In an embodiment, the growth-enhancing molecule is selected from the group consisting of: collagen, fibronectin, a growth factor, and an antibody to a stem cell surface receptor.

In an embodiment, stimulating includes culturing the ICP with at least one factor derived from a sample tissue.

In an embodiment, the method includes preparing a conditioned medium for culturing the ICP therein, the conditioned medium including the factor, the factor being derived from the tissue, the tissue being selected from the group consisting of: peripheral nerve tissue, central nervous system (CNS) tissue, retinal tissue, pigment epithelial tissue, photoreceptor tissue, fetal retinal tissue, embryonic retinal tissue, mature retinal tissue, blood vessel tissue, cardiac tissue, pancreatic endocrine tissue, pancreatic exocrine tissue, smooth muscle tissue, lymphatic tissue, hepatic tissue, lung tissue, skin tissue, exocrine glandular tissue, mammary gland tissue, endocrine glandular tissue, thyroid gland tissue, pituitary gland tissue, and plant tissue.

In an embodiment, stimulating includes co-culturing the ICP with a sample tissue.

In an embodiment, co-culturing includes preparing the sample tissue by a method selected from the group consisting of slicing the sample tissue, and homogenizing the sample issue.

In an embodiment, co-culturing includes:

utilizing the sample tissue to produce a conditioned medium; and co-culturing the ICP with the sample tissue in the conditioned medium.

In an embodiment, co-culturing includes separating the sample tissue from the ICP by a semi-permeable membrane.

In an embodiment, designating the sample tissue to include a tissue selected from the group consisting of: peripheral nerve tissue, central nervous system (CNS) tissue, retinal tissue, pigment epithelial tissue, photoreceptor tissue, fetal retinal tissue, embryonic retinal tissue, mature retinal tissue, blood vessel tissue, cardiac tissue, pancreatic endocrine tissue, pancreatic exocrine tissue, smooth muscle tissue, lymphatic tissue, hepatic tissue, lung tissue, skin tissue, exocrine glandular tissue, mammary gland tissue, endocrine glandular tissue, thyroid gland tissue, pituitary gland tissue, and plant tissue.

In an embodiment, the method includes systemically administering the PCP to a patient.

In an embodiment, the method includes locally administering the PCP to a site of the patient including injured tissue.

In an embodiment, locally administering the PCP includes implanting at the site a device including the PCP.

In an embodiment, the device includes at least one item selected from the group consisting of a metal, a plastic, a glass, and a biodegradable element, and implanting the device includes implanting the device including the selected item.

In an embodiment, the method includes using the device to enable increased survival of PCP in injured tissue

In an embodiment, the method includes configuring the device for slow release of cells of the PCP into the injured tissue.

In an embodiment, the method includes secreting, from the PCP, therapeutic molecules to the tissue.

In an embodiment, the method includes secreting, from the device, soluble molecules that support the PCP.

There is also provided, in accordance with an embodiment of the invention, apparatus for implantation in a patient, including a medical device including a PCP produced according to any of the procedures described herein for producing a PCP.

In an embodiment, the medical device includes a chamber having the PCP disposed therein, and a membrane, through which molecules generated by the PCP are able to pass.

There is further provided, in accordance with an embodiment of the invention, a method including in vitro stimulating an initiating cell population (ICP) of at least 5 million cells that have a density of less than 1.072 g/ml, and at least 1% of which are CD34+CD45−/Dim, to differentiate into a progenitor/precursor cell population (PCP).

There is also provided, in accordance with an embodiment of the invention, a method including in vitro stimulating an initiating cell population (ICP) of at least ten thousand cells that have a density of less than 1.072 g/ml to differentiate into a progenitor/precursor cell population (PCP).

There is further provided, in accordance with an embodiment of the invention, a method including separating lower density cells from higher density cells, the lower density cells defining an initiating cell population (ICP), and in vitro stimulating the ICP to differentiate into a progenitor/precursor cell population (PCP).

In an embodiment, the ICP includes at least 5 million cells, and wherein stimulating the ICP includes stimulating the ICP that includes the at least 5 million cells.

In an embodiment, at least 1.5% of the cells of the ICP are CD34+CD45−/Dim, and wherein stimulating the ICP includes stimulating the ICP of which at least 1.5% of the cells are CD34+CD45−/Dim.

In an embodiment, at least 2% of the cells of the ICP are CD34+CD45−/Dim, and wherein stimulating the ICP includes stimulating the ICP of which at least 2% of the cells are CD34+CD45−/Dim.

In an embodiment, at least 30% of the cells of the ICP are CD31Bright, and wherein stimulating the ICP includes stimulating the ICP of which at least 30% of the cells are CD34+CD45−/Dim.

In an embodiment, the ICP includes at least 5 million cells that have a density of less than 1.062 g/ml, at least 1% of which are CD34+CD45−/Dim, and wherein stimulating the ICP includes stimulating the ICP that has the at least 5 million cells that have a density of less than 1.062 g/ml.

In an embodiment, at least 50% of cells in the ICP are CD31Bright, and wherein stimulating the ICP includes stimulating the ICP of which at least 50% of cells therein are CD31Bright.

In an embodiment, the method includes preparing the PCP as a product for administration to a patient.

In an embodiment, the method includes preparing the PCP as a research tool.

In an embodiment, stimulating the ICP includes only stimulating the ICP if the ICP is derived from a mammalian donor.

In an embodiment, the method includes applying cells extracted from a mammalian donor to one or more gradients suitable for selecting cells having a density less than 1.072 g/ml, and deriving the ICP from the cells applied to the gradient.

In an embodiment, the ICP is characterized by at least 2.5% of the ICP being CD34+CD45−/Dim, and wherein stimulating the ICP includes stimulating the ICP having the at least 2.5% of the ICP that are CD34+CD45−/Dim.

In an embodiment, the ICP is characterized by at least 50% of the ICP being CD31Bright, and wherein stimulating the ICP includes stimulating the ICP having the at least 50% of the ICP that are CD31Bright.

In an embodiment, the ICP is characterized by at least 40% of the ICP being CD31Bright, and wherein stimulating the ICP includes stimulating the ICP having the at least 40% of the ICP that are CD31Bright.

In an embodiment, stimulating the ICP includes stimulating the ICP to differentiate into a pre-designated, desired class of progenitor cells.

In an embodiment, the method includes deriving the ICP from at least one source selected from the group consisting of: embryonic tissue, fetal tissue, umbilical cord blood, umbilical cord tissue, neonatal tissue, adult tissue, bone marrow, mobilized blood, peripheral blood, peripheral blood mononuclear cells, skin cells, and plant tissue.

In an embodiment, the method includes deriving the ICP from at least one source selected from the group consisting of: fresh tissue and frozen tissue.

In an embodiment, the method includes identifying an intended recipient of the PCP, and deriving the ICP from at least one source selected from the group consisting of: tissue autologous to tissue of the intended recipient, tissue syngeneic to tissue of the intended recipient, tissue allogeneic to tissue of the intended recipient, and tissue xenogeneic to tissue of the intended recipient.

In an embodiment, stimulating the ICP includes culturing the ICP for a period lasting between 1 and 5 days in a culture medium including less than 5% serum.

In an embodiment, stimulating the ICP includes culturing the ICP for a period lasting between 1 and 5 days in a culture medium including at least 10% serum.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including a factor selected from the group consisting of: erythropoietin, a statin, and an antidiabetic agent.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including a factor selected from the group consisting of: estrogen, prolactin, progestin, an adrenocorticoid hormone, ACTH, and cortisone.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including a factor selected from the group consisting of: anti-Tie-2, anti-CD133, and anti-CD 117.

In an embodiment, stimulating the ICP includes culturing the ICP in the presence of a factor selected from the group consisting of: erythropoietin, a statin, an antidiabetic agent, a thiazolidinedione, rosiglitazone, a proliferation-differentiation-enhancing agent, anti-CD34, anti-Tie-2, anti-CD133, anti-CD117, LIF, EPO, IGF, b-FGF, M-CSF, GM-CSF, TGF alpha, TGF beta, VEGF, BHA, BDNF, GDNF, NGF, NT3, NT4/5, S-100, CNTF, EGF, NGF3, CFN, ADMIF, estrogen, prolactin, an adrenocorticoid hormone, ACTH, MCT-165, glatiramer acetate, a glatiramer acetate-like molecule, IFN alpha, IFN beta or any other immunoregulatory agent, glutamate, serotonin, acetylcholine, NO, retinoic acid (RA) or any other vitamin D derivative, heparin, insulin, and forskolin, cortisone.

In an embodiment, the method includes preparing the ICP, and facilitating a diagnosis responsive to a characteristic of the preparation of the ICP.

In an embodiment, the method includes freezing the ICP prior to stimulating the ICP.

In an embodiment, the method includes freezing the PCP.

In an embodiment, the method includes transporting the ICP to a site at least 10 km from a site where the ICP is first created, and stimulating the ICP at the remote site.

In an embodiment, the method includes transporting the PCP to a site at least 10 km from a site where the PCP is first created.

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million PCP cells.

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that at least 1.5% of cells of the PCP demonstrate a feature selected from the group consisting of: a desired morphology, a desired cellular marker, a desired cellular component, a desired enzyme, a desired receptor, a desired genotypic feature, and a desired physiological feature.

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million angiogenic cell precursors (ACPs).

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million cardiomyocyte progenitors.

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million neural cell progenitors.

In an embodiment, the method includes transfecting into the PCP a gene identified as suitable for gene therapy.

In an embodiment, the method includes transfecting a gene into the PCP, and subsequently assessing a level of expression of the gene.

In an embodiment, the method includes transfecting a gene into the ICP, and subsequently assessing a level of expression of the gene.

In an embodiment, stimulating the ICP includes culturing the ICP during a period of between 2 and 120 days.

In an embodiment, stimulating the ICP includes culturing the ICP during a period of between 3 and 60 days.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including less than 10% serum, for a duration of between 1 and 120 days.

In an embodiment, stimulating the ICP includes culturing the ICP in a culture medium including at least 10% serum, for a duration of between 1 and 120 days.

In an embodiment, the method includes characterizing the PCP as including angiogenic cell precursors (ACPs), in response to an evaluation of at least a feature selected from the group consisting of: a phenotypical feature of cells in the PCP, a genotypical feature of cells in the PCP, and a physiological feature of cells in the PCP.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an evaluation of at least two of the features.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an evaluation of each of the features.

In an embodiment:

the phenotypical feature includes a morphological feature selected from the group consisting of: a cell size larger than 20 μm, an elongated cell, a spindle-shaped cell, an irregularly-shaped cell, a granulated cell, a cell including an enlarged dark nucleus, a multinuclear cell, a cell including flagella-like structures, a cell including pseudopodia, and a cell having a polygonal shape; and

characterizing the PCP includes characterizing the PCP in response to an evaluation of the selected morphological feature.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells of the PCP have the selected feature.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an identification in the PCP of a feature selected from the group consisting of: CD31Bright, CD34, CD117, CD133, Tie-2, CD34+CD133+, KDR, CD34+KDR+, CD144, von Willebrand Factor, SH2 (CD105), SH3, fibronectin, collagen type I, collagen type III, collagen type IV, ICAM type 1, ICAM type 2, VCAM1, vimentin, BMP-R IA, BMP-RIL CD44, integrin b1, aSM-actin, MUC18, and CXCR4.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells of the PCP have the selected feature.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an assessment of uptake by the PCP of Ac-LDL.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells of the PCP demonstrate uptake of Ac-LDL.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells that are CD31Bright demonstrate uptake of Ac-LDL.

In an embodiment, characterizing the PCP includes assessing secretion by the PCP of a molecule selected from the group consisting of: IL-8, angiogenin, VEGF, MMP2, and MMP9.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells of the PCP secrete the selected molecule.

In an embodiment, characterizing the PCP includes culturing a portion of the PCP on a semi-solid extracellular matrix (ECM), and identifying in the cultured portion a feature selected from the group consisting of: a tube-like structure, a colony, a cluster, and a tendency to migrate towards a chemoattractant.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells in the cultured portion have a property selected from the group consisting of: formation of a tube-like structure, an ability to form a colony, a cluster, and a tendency to migrate towards a chemoattractant.

In an embodiment, the method includes including identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million ACPs.

In an embodiment, the method includes characterizing the PCP as including a cardiomyocyte (CMC) PCP in response to an evaluation of a feature selected from the group consisting of: a phenotypic feature of cells in the PCP, a genotypic feature on the cells in the PCP, and a physiological feature of cells in the PCP.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an evaluation of at least two of the features.

In an embodiment, the method includes characterizing the PCP includes characterizing the PCP in response to an evaluation of each of the features.

In an embodiment, the phenotypic feature includes a morphological feature selected from the group consisting of: a cell size larger than 20 μm, an elongated cell, an irregularly-shaped cell, a granulated cell, a cell including an enlarged dark nucleus, a multinuclear cell, a cell with dark cytoplasm, and cells arranged in parallel to each other; and

wherein characterizing the PCP includes characterizing the PCP in response to an evaluation of the selected morphological feature.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an identification in the PCP of a feature selected from the group consisting of: CD31, CD117, sarcomeric alpha-actin, beta-actin, alpha-actinin, desmin, cardiac troponin T, Connexin-43, alpha/beta-MHC, sarcomeric alpha-tropomyosin, Troponin I, GATA-4, Nkx2.5/Csx, MLC-2, and MEF-2.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an identification of the PCP as expressing a gene for a factor selected from the group consisting of sarcomeric alpha-actin, beta-actin, alpha-actinin, desmin, cardiac troponin T, Connexin-43, alpha/beta-MHC, sarcomeric, alpha-tropomyosin, Troponin I, GATA-4, Nkx2.5/Csx, MLC-2 and MEF-2.

In an embodiment, the method includes identifying the PCP as being suitable for therapeutic implantation in response to an assessment that the PCP includes at least 1 million CMC progenitors.

In an embodiment, characterizing the PCP includes identifying that at least 1.5% of cells of the PCP have a characteristic selected from the group consisting of a CMC-progenitor morphological characteristic, expression of a CMC-associated cellular marker, expression of a CMC-progenitor gene product, and expression of a CMC-progenitor physiological feature.

In an embodiment, characterizing the PCP includes characterizing the PCP in response to an identification in the PCP of an action in response to activation of the PCP, the action selected from the group consisting of: increasing intracellular Ca2⁺ level, generating membranal electrophysiological action potentials, and mechanical cellular contraction in vitro.

In an embodiment, the method includes activating the PCP to produce the selected action, using a technique selected from the group consisting of: electrical activation of the PCP, and chemical activation of the PCP.

In an embodiment, the method includes:

assessing a phenotypic aspect of the PCP and a genotypic aspect of the PCP and a physiological aspect of the PCP; and

designating the PCP as being suitable for implantation in a patient in response to each of the assessments.

In an embodiment, assessing the phenotypic aspect of the PCP includes assessing an aspect of the PCP selected from the group consisting of: morphology of the PCP, a cellular marker of cells of the PCP, an enzyme of the PCP, a coenzyme of the PCP, and presence of a designated cellular receptor on cells of the PCP.

In an embodiment, assessing the genotypic aspect of the PCP includes assessing an aspect of the PCP selected from the group consisting of: production of a gene by cells of the PCP, expression of a gene by cells of the PCP, and generation of a gene product by cells of the PCP.

In an embodiment, assessing the physiological aspect of the PCP includes assessing an aspect of the PCP selected from the group consisting of: secretion of soluble molecules by cells of the PCP, generation of signals by cells of the PCP, response by cells of the PCP to signals, and an enzymatic reaction performed by cells of the PCP.

In an embodiment, the method includes facilitating a diagnosis responsive to stimulating the ICP to differentiate into the PCP.

In an embodiment, facilitating the diagnosis includes assessing an extent to which the stimulation of the ICP produces a particular characteristic of the PCP.

In an embodiment, the method includes transfecting a gene into the ICP prior to stimulating the ICP.

In an embodiment, transfecting the gene includes transfecting into the ICP a gene identified as suitable for gene therapy.

In an embodiment, the method includes preparing, as a product for administration to a patient, the PCP generated by differentiation of the ICP into which the gene has been transfected.

In an embodiment, the method includes stimulating the ICP includes incubating the ICP in a container having a surface including a growth-enhancing factor.

In an embodiment, the method includes the growth-enhancing factor is selected from the group consisting of: collagen, plasma, fibronectin, a growth factor, tissue-derived extra cellular matrix, and an antibody to a stem cell surface receptor.

In an embodiment, stimulating the ICP includes incubating the ICP in a container with a surface including a growth-enhancing molecule other than collagen or fibronectin.

In an embodiment, incubating the ICP includes incubating the ICP in a container having a surface that includes, in addition to the growth-enhancing molecule, at least one of: collagen and fibronectin.

In an embodiment, the method includes mixing the growth-enhancing molecule with the at least one of: collagen and fibronectin.

In an embodiment, the method includes applying to the surface a layer that includes the growth-enhancing molecule and a separate layer that includes the at least one of: collagen and fibronectin.

In an embodiment, stimulating the ICP includes:

during a low-serum time period, culturing the ICP in a culture medium including less than 10% serum; and

during a high-serum time period, culturing the ICP in a culture medium including greater than or equal to 10% serum.

In an embodiment, culturing the ICP during the low-serum time period includes culturing the ICP for a duration of between 1 and 60 days.

In an embodiment, culturing the ICP during the low-serum time period includes culturing the ICP for a duration of between 1 and 5 days.

In an embodiment, culturing the ICP during the high-serum time period includes culturing the ICP for a duration of between 1 and 120 days.

In an embodiment, culturing the ICP during the high-serum time period includes culturing the ICP for a duration of between 1 and 60 days.

In an embodiment, culturing the ICP during the low-serum time period is performed prior to culturing the ICP during the high-serum time period.

In an embodiment, culturing the ICP during the low-serum time period is performed following culturing the ICP during the high-serum time period.

In an embodiment, the method includes:

during a hypoxic time period lasting at least 2, hours, culturing the ICP under hypoxic conditions; and

during a non-hypoxic time period lasting at least 1 day, culturing the ICP under non-hypoxic conditions.

In an embodiment, the hypoxic and non-hypoxic time-periods are within a culturing time period lasting less than 30 days, and wherein culturing the ICP under hypoxic conditions includes culturing the cells under hypoxic conditions during a first two days of the culturing time period.

In an embodiment, the hypoxic and non-hypoxic time-periods are within a culturing time period lasting less than 30 days, and wherein culturing the ICP under hypoxic conditions includes culturing the ICP under hypoxic conditions during a last two days of the culturing time period.

In an embodiment, the hypoxic and non-hypoxic time-periods are within a culturing time period lasting less than 30 days, and wherein culturing the ICP under hypoxic conditions includes culturing the ICP under hypoxic conditions for at least 2 hours between a first two days and a last two days of the culturing time period.

In an embodiment, culturing the ICP under hypoxic conditions is performed prior to culturing the ICP under non-hypoxic conditions.

In an embodiment, culturing the ICP under hypoxic conditions is performed following culturing the ICP under non-hypoxic conditions.

In an embodiment, stimulating the ICP includes:

culturing the ICP in a first container during a first portion of a culturing period;

removing at least some cells of the ICP from the first container at the end of the first portion of the period; and

culturing, in a second container during a second portion of the period, the cells removed from the first container.

In an embodiment, the method includes, subsequently to the step of culturing in the second container:

culturing the ICP in a primary container during a first portion of an additional culturing period;

removing at least some cells of the ICP from the primary container at the end of the first portion of the additional period; and

culturing, in a secondary container during a second portion of the additional period, the cells removed from the primary container.

In an embodiment, stimulating the ICP includes:

culturing the ICP in a first container during a first portion of a culturing period;

removing cells of the ICP from the first container at the end of the first portion of the period; and

culturing, in a second container during a second portion of the period, the cells removed from the first container.

In an embodiment, removing at least some cells of the ICP includes selecting for removal cells that adhere to a surface of the first container.

In an embodiment, removing at least some cells of the ICP includes selecting for removal cells that do not adhere to a surface of the first container.

In an embodiment, the first container includes on a surface thereof a growth-enhancing molecule, and wherein culturing the ICP in the first container includes culturing the ICP in the first container that includes the growth-enhancing molecule.

In an embodiment, the growth-enhancing molecule is selected from the group consisting of: collagen, plasma, fibronectin, a growth factor, tissue-derived extra cellular matrix and an antibody to a stem cell surface receptor.

In an embodiment, the second container includes on a surface thereof a growth-enhancing molecule, and wherein culturing the ICP in the second container includes culturing the ICP in the second container that includes the growth-enhancing molecule.

In an embodiment, the growth-enhancing molecule is selected from the group consisting of: collagen, fibronectin, a growth factor, and an antibody to a stem cell surface receptor.

In an embodiment, stimulating includes culturing the ICP with at least one factor derived from a sample tissue.

In an embodiment, the method includes preparing a conditioned medium for culturing the ICP therein, the conditioned medium including the factor, the factor being derived from the tissue, the tissue being selected from the group consisting of: peripheral nerve tissue, central nervous system (CNS) tissue, retinal tissue, pigment epithelial tissue, photoreceptor tissue, fetal retinal tissue, embryonic retinal tissue, mature retinal tissue, blood vessel tissue, cardiac tissue, pancreatic endocrine tissue, pancreatic exocrine tissue, smooth muscle tissue, lymphatic tissue, hepatic tissue, lung tissue, skin tissue, exocrine glandular tissue, mammary gland tissue, endocrine glandular tissue, thyroid gland tissue, pituitary gland tissue, and plant tissue.

In an embodiment, stimulating includes co-culturing the ICP with a sample tissue.

In an embodiment, co-culturing includes preparing the sample tissue by a method selected from the group consisting of: slicing the sample tissue, and homogenizing the sample issue.

In an embodiment, co-culturing includes:

utilizing the sample tissue to produce a conditioned medium; and

co-culturing the ICP with the sample tissue in the conditioned medium.

In an embodiment, co-culturing includes separating the sample tissue from the ICP by a semi-permeable membrane.

In an embodiment, the method includes designating the sample tissue to include a tissue selected from the group consisting of: peripheral nerve tissue, central nervous system (CNS) tissue, retinal tissue, pigment epithelial tissue, photoreceptor tissue, fetal retinal tissue, embryonic retinal tissue, mature retinal tissue, blood vessel tissue, cardiac tissue, pancreatic endocrine tissue, pancreatic exocrine tissue, smooth muscle tissue, lymphatic tissue, hepatic tissue, lung tissue, skin tissue, exocrine glandular tissue, mammary gland tissue, endocrine glandular tissue, thyroid gland tissue, pituitary gland tissue, and plant tissue.

There is further provided, in accordance with an embodiment of the invention, a method for treating a patient, including:

identifying a patient having a sexual dysfunction; and

administering angiogenic cell precursors to the patient, in order to treat the dysfunction.

There is also provided, in accordance with an embodiment of the present invention, a method including in vitro stimulating a core cell population (CCP) of at least 5 million cells that have a density of less than 1.072 g/ml, and at least 1% or at least 2% of which are CD34+CD45−/Dim, to differentiate into a progenitor/precursor cell population (PCP).

For some applications, the CCP includes at least 5 million cells that have a density of less than 1.062 g/ml, at least 2% of which are CD34+CD45−/Dim, and stimulating the CCP includes stimulating the CCP that has the at least 5 million cells that have a density of less than 1.062 g/ml.

For some applications, the method includes preparing the PCP as a product for administration to a patient. Alternatively, the method includes preparing the PCP as a research tool or a diagnostic tool.

For some applications, stimulating the CCP includes only stimulating the CCP if the CCP is derived from a mammalian donor. For some applications, the method includes applying cells extracted from a mammalian donor to one or more gradients suitable for selecting cells having a density less than 1.072 g/ml, and deriving the CCP from the cells applied to the gradient.

For some applications, the CCP is characterized by at least 2.5% of the CCP being CD34+CD45−/Dim, and stimulating the CCP includes stimulating the CCP having the at least 2.5% of the CCP that are CD34+CD45−/Dim. For some applications, the CCP is characterized by at least 50% of the CCP being CD31Bright, and stimulating the CCP includes stimulating the CCP having the at least 50% of the CCP that are CDC31Bright+. For some applications, the CCP is characterized by at least 40% of the CCP being CD31Bright, and stimulating the CCP includes stimulating the CCP having the at least 40% of the CCP that are CD31Bright.

For some applications, stimulating the CCP includes stimulating the CCP to differentiate into a pre-designated, desired class of progenitor cells.

For some applications, stimulating the CCP includes culturing the CCP during a period of between 3 and 30, 60, or 120 days.

For some applications, the method includes deriving the CCP from at least one source selected from the group consisting of: embryonic tissue, fetal tissue, umbilical cord blood, umbilical cord tissue, neonatal tissue, adult tissue, bone marrow, mobilized blood, peripheral blood, peripheral blood mononuclear cells, skin cells, and plant tissue. Alternatively, the method includes deriving the CCP from at least one source selected from the group consisting of: fresh tissue and frozen tissue. For some applications, the method includes identifying an intended recipient of the PCP, and deriving the CCP from at least one source selected from the group consisting of: tissue autologous to tissue of the intended recipient, tissue syngeneic to tissue of the intended recipient, tissue allogeneic to tissue of the intended recipient, and tissue xenogeneic to tissue of the intended recipient.

For some applications, stimulating the CCP includes incubating the CCP in a container having a surface including an antibody.

For some applications, stimulating the CCP includes incubating the CCP in a container having a surface including a plasma.

For some applications, stimulating the CCP includes culturing the CCP for a period lasting between 1 and 5, 10, or 20 days in a culture medium including less than 5% serum. For some applications, stimulating the CCP includes culturing the CCP for a period lasting between 1 and 5, 10, or 20 days in a culture medium including at least 10% serum.

For some applications, stimulating the CCP includes culturing the CCP in the presence of at least one of the following: erythropoietin, a statin, an antidiabetic agent, a thiazolidinedione, rosiglitazone, a proliferation-differentiation-enhancing agent, anti-CD34, anti-Tie-2, anti-CD133, anti-CD117, LIF, EPO, IGF, b-FGF, M-CSF, GM-CSF, TGF alpha, TGF beta, VEGF, BHA, BDNF, NGF, NT3, NT4/5, GDNF, S-100, CNTF, EGF, NGF3, CFN, ADMIF, prolactin, an adrenocorticoid hormone, ACTH, glutamate, serotonin, acetylcholine, NO, retinoic acid (RA) or any other vitamin D derivative, heparin, insulin, forskolin, cortisone, cortisol, dexamethasone, estrogen, a steroid, MCDB-201, MCT-165, glatiramer acetate, a glatiramer acetate-like molecule, IFN alpha, IFN beta or any other immunoregulatory agent, sodium selenite, linoleic acid, ascorbic acid, transferrin, 5-azacytidine, PDGF, VEGF, cardiotrophin, and thrombin.

For some applications, the method includes preparing the CCP, and facilitating a diagnosis responsive to a characteristic of the preparation of the CCP.

For some applications, the method includes freezing the CCP prior to stimulating the CCP. For some applications, the method includes freezing the PCP.

For some applications, the method includes transporting the CCP to a site at least 10 km from a site where the CCP is first created, and stimulating the CCP at the remote site. For some applications, the method includes transporting the PCP to a site at least 10 km from a site where the PCP is first created.

In an embodiment, the method includes facilitating a diagnosis responsive to stimulating the CCP to differentiate into the PCP. For some applications, facilitating the diagnosis includes assessing an extent to which the stimulation of the CCP produces a particular characteristic of the PCP.

In an embodiment, the method includes transfecting a gene into the CCP prior to stimulating the CCP. For some applications, the method includes preparing, as a product for administration to a patient, the PCP generated by differentiation of the CCP into which the gene has been transfected.

In an embodiment, the method includes transfecting a gene into the PCP prior to administration of the PCP to a patient.

In an embodiment, stimulating the CCP includes incubating the CCP in a container with a surface including a growth-enhancing molecule other than collagen or fibronectin. For some applications, incubating the CCP cells includes incubating the CCP in a container having a surface that includes, in addition to the growth-enhancing molecule, at least one of collagen, plasma and fibronectin. For some applications, the method includes mixing the growth-enhancing molecule with the at least one of: collagen, plasma and fibronectin. For some applications, the method includes applying to the surface a layer that includes the growth-enhancing molecule and a separate layer that includes the at least one of: collagen, plasma and fibronectin.

In an embodiment, stimulating the. CCP includes:

during a low-serum time period, culturing the CCP in a culture medium including less than 10% serum; and

during a high-serum time period, culturing the CCP in a culture medium including greater than or equal to 10% serum.

For some applications, culturing the CCP during the low-serum time period includes culturing the CCP for a duration of between 1 and 5 or 20 days. For some applications, culturing the CCP during the high-serum time period includes culturing the CCP for a duration of between 1 and 30, 60, or 120 days. For some applications, culturing the CCP during the low-serum time period is performed prior to culturing the CCP during the high-serum time period. For some applications, culturing the CCP during the low-serum time period is performed following culturing the CCP during the high-serum time period.

In an embodiment, the method includes:

during a hypoxic time period lasting at least 2 hours, culturing the CCP under hypoxic conditions; and

during a non-hypoxic time period lasting at least 1 day, culturing the CCP under non-hypoxic conditions.

For some applications, the hypoxic and non-hypoxic time-periods are within a culturing time period lasting less than 120 days (e.g., less than 30 days), and culturing the CCP under hypoxic conditions includes culturing the cells under hypoxic conditions during a first two days of the culturing time period. For some applications, the hypoxic and non-hypoxic time-periods are within a culturing time period lasting less than 120 days (e.g., less than 30 days), and culturing the CCP under hypoxic conditions includes culturing the CCP under hypoxic conditions during a last two days of the culturing time period. For some applications, the hypoxic and non-hypoxic time-periods are within a culturing time period lasting less than 120 days (e.g., less than 30 days), and culturing the CCP under hypoxic conditions includes culturing the CCP under hypoxic conditions for at least 2 hours between a first two days and a last two days of the culturing time period.

For some applications, culturing the CCP under hypoxic conditions is performed prior to culturing the CCP under non-hypoxic conditions. Alternatively, culturing the CCP under hypoxic conditions is performed following culturing the CCP under non-hypoxic conditions.

In an embodiment, stimulating the CCP includes:

culturing the CCP in a first container during a first portion of a culturing period;

removing all or at least some cells of the CCP from the first container at the end of the first portion of the period; and

culturing, in a second container during a second portion of the period, the cells removed from the first container.

For some applications, removing at least some cells of the CCP includes selecting for removal cells that adhere to a surface of the first container. For some applications, removing at least some cells of the CCP includes selecting for removal cells that do not adhere to a surface of the first container.

For some applications, the first container includes on a surface thereof a growth-enhancing molecule, and culturing the CCP in the first container includes culturing the CCP in the first container that includes the growth-enhancing molecule.

For some applications, the growth-enhancing molecule is selected from the group consisting of: collagen, plasma, fibronectin, a growth factor, tissue-derived extra cellular matrix and an antibody to a stem cell surface receptor.

For some applications, the second container includes on a surface thereof a growth-enhancing molecule, and culturing the CCP in the second container includes culturing the CCP in the second container that includes the growth-enhancing molecule.

For some applications, the growth-enhancing molecule is selected from the group consisting of collagen, plasma, fibronectin, a growth factor, tissue-derived extra cellular matrix and an antibody to a stem cell surface receptor.

In an embodiment, stimulating includes culturing the CCP with at least one factor derived from a target tissue. For some applications, the method includes preparing a conditioned medium for culturing the CCP therein, the conditioned medium including the factor, the factor being derived from a tissue selected from the group consisting of: peripheral nerve tissue, central nervous system (CNS) tissue, retinal tissue, pigment epithelial tissue, photoreceptor tissue, fetal retinal tissue, embryonic retinal tissue, mature retinal tissue, blood vessel tissue, cardiac tissue, pancreatic endocrine tissue, pancreatic exocrine tissue, smooth muscle tissue, lymphatic tissue, hepatic tissue, lung tissue, skin tissue, exocrine glandular tissue, mammary gland tissue, endocrine glandular tissue, thyroid gland tissue, pituitary gland tissue, and plant tissue.

In an embodiment, stimulating includes co-culturing the CCP with a tissue. For some applications, co-culturing includes preparing a target tissue by a method selected from the group consisting of: slicing the target tissue, and homogenizing the target issue. For some applications, co-culturing includes utilizing the target tissue to produce a conditioned medium, and co-culturing the CCP with the target tissue in the conditioned medium. For some applications, co-culturing includes separating the target tissue from the CCP by a semi-permeable membrane.

For some applications, the method includes designating a tissue for co-culture purposes to include a tissue selected from the group consisting of: peripheral nerve tissue, central nervous system (CNS) tissue, retinal tissue, pigment epithelial tissue, photoreceptor tissue, fetal retinal tissue, embryonic retinal tissue, mature retinal tissue, blood vessel tissue, cardiac tissue, pancreatic endocrine tissue, pancreatic exocrine tissue, smooth muscle tissue, lymphatic tissue, hepatic tissue, lung tissue, skin tissue, exocrine glandular tissue, mammary gland tissue, endocrine glandular tissue, thyroid gland tissue, pituitary gland tissue, and plant tissue.

There is also provided, in accordance with an embodiment of the present invention, a method including in vitro stimulating an elemental cell population (ECP) of at least 5 million cells that have a density of less than 1.072 g/ml, at least 1.5% of which are CD34+CD45−/Dim, and at least 30% of which are CD31Bright, to differentiate into a progenitor/precursor cell population (PCP).

For some applications, the present invention includes treating a patient with a PCP administrated systemically.

For some applications, the present invention includes treating a patient with a PCP administrated locally to injured tissue.

There is also provided, in accordance with an embodiment of the present invention, a method for treating a patient including administering a PCP using an implantable medical device, which, in an embodiment, includes metal, plastic, glass, or another material, and which for some applications is biodegradable. As appropriate for a given application, the medical device may include a stent, microparticles, or microcapsules.

There is also provided, in accordance with an embodiment of the present invention, a method comprising implanting, at a site including injured tissue, a medical device including a PCP, to enable increased survival at the site of the PCP.

There is also provided, in accordance with an embodiment of the present invention, a method including a medical device that provides slow release of a PCP into injured tissue.

There is also provided, in accordance with an embodiment of the present invention, a method including coupling a PCP to a medical device, wherein the PCP is adapted to be a source of therapeutic soluble molecules to a subject in whom the medical device is implanted. For some applications, apparatus comprises a chamber having disposed therein a population of stem cells (e.g., a PCP produced using techniques described herein), the chamber being surrounded by a semi-permeable membrane. Therapeutic molecules leave the chamber through the membrane, and treat the patient. As appropriate, techniques and apparatus described in the above-referenced US Patent Application Publication 2005/0209556 to Tresco and article by Rehman may be practiced in combination with this embodiment, mutatis mutandis.

There is also provided, in accordance with an embodiment of the present invention, a method including attaching a PCP to a medical device, wherein the medical device is a source of soluble molecules that support the PCP.

There is additionally provided, in accordance with an embodiment of the present invention, a composition of matter, including a population of cultured cells that includes a sub-population of cells that both stain as CD31Bright and demonstrate uptake of Ac-LDL+.

In an embodiment, the sub-population secretes IL-8.

In an embodiment, the sub-population secretes at least 50 pg IL-8 per 10⁶ cells/ml over a period of at least 24 hours.

In an embodiment, the sub-population secretes at least 150 pg IL-8 per 10⁶ cells/nal over a period of at least 24 hours.

In an embodiment, the sub-population secretes at least 1000 pg per 10⁶ cells/ml over a period of at least 24 hours.

In an embodiment, at least 1.5% of the cells of the population secrete a molecule selected from the group consisting of: IL-8, angiogenin, VEGF, MMP2, and MMP9.

In an embodiment, at least 1.5% of the cells of the population have a tendency to migrate toward a chemoattractant selected from the group consisting of: bFGF, VEGF, SCF, G-CSF, GM-CSF, SDF-1, and IL-8.

There is further provided, in accordance with an embodiment of the present invention, a composition of matter, including a population of cultured cells that includes a sub-population of cells that stain as CD31Bright, demonstrate uptake of Ac-LDL+ and secrete interleukin-8.

In an embodiment, the sub-population includes at least 10% of the cells in the population.

In an embodiment, the sub-population includes at least 25% of the cells in the population.

In an embodiment, the sub-population includes at least 50% of the cells in the population.

In an embodiment, the sub-population secretes at least 50 pg IL-8 per 10⁶ cells/ml over a period of at least 24 hours.

In an embodiment, the sub-population secretes at least 150 pg IL-8 per 10⁶ cells/ml over a period of at least 24 hours.

In an embodiment, the sub-population secretes at least 1000 pg IL-8 per 10⁶ cells/ml over a period of at least 24 hours.

In an embodiment, at least 1.5% of the cells of the population include a morphological feature selected from the group consisting of: a cell size larger than 20 um, an elongated cell, a spindle-shaped cell, an irregularly-shaped cell, a granulated cell, a cell including an enlarged dark nucleus, a multinuclear cell, a cell including flagella-like structures, a cell including pseudopodia, and a cell having a polygonal shape.

In an embodiment, at least 1.5% of the cells of the population include a feature selected from the group consisting of CD34, CD117, CD133, Tie-2, CD34+CD133+, KDR, CD34+KDR+, CD144, von Willebrand Factor, SH2 (CD105), SH3, fibronectin, collagen type I, collagen type III, collagen type IV, ICAM type 1, ICAM type 2, VCAM1, vimentin, BMP-R IA, BMP-RII, CD44, integrin b1, aSM-actin, MUC18, CXCR4 and CXCR8.

In an embodiment, at least 1.5% of the cells of the population secrete a molecule selected from the group consisting of angiogenin, VEGF, MMP2, and MMP9.

In an embodiment, at least 1.5% of the cells of the population include a feature selected from the group consisting of: a tube-like structure, a tendency to form a colony, a tendency to form a cluster, and a tendency to migrate towards chemoattractants selected from the group consisting of: bFGF, VEGF, SCF, G-CSF, GM-CSF, SDF-1, and IL-8.

In an embodiment, characterizing the PCP includes culturing at least a portion of the PCP on a surface, and identifying a tendency of the at least a portion of the PCP to migrate toward IL-8.

The present invention will be more fully understood from the following detailed description of embodiments thereof, taken together with the drawings, in which:

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graph showing results obtained from CCP cells in one representative experiment, in accordance with an embodiment of the present invention;

FIG. 2 is a photograph showing morphology of angiogenic cell precursor cells, produced in accordance with an embodiment of the present invention;

FIG. 3 is a photograph characterizing uptake of Ulex-Lectin and staining with CD31 stain of an ACP-rich PCP, produced in accordance with an embodiment of the present invention;

FIG. 4 is a photograph characterizing uptake of Ac-LDL and staining with CD31 stain of an ACP-rich PCP, produced in accordance with an embodiment of the present invention;

FIG. 5 is a photograph showing tube formation in an ACP-rich PCP, produced in accordance with an embodiment of the present invention;

FIGS. 6A and 6B are graphs showing migration of Ac-LDL-DiO pre-labeled ACPs in response to hIL-8, in accordance with an embodiment of the present invention;

FIG. 7 is a graph showing migration of Ac-LDL-DiO pre-labeled ACPs in response to a cultured medium, in accordance with an embodiment of the present invention;

FIG. 8 is a graph of migration of PBMC cells in response to hIL-8, in accordance with an embodiment of the present invention;

FIGS. 9A and 9B are graphs showing experimental results of improved ejection fraction and reduced necrosis in response to injection of ACP cells in accordance with an embodiment of the present invention;

FIGS. 9C, 9D, and 9E are photographs showing sections taken from a rat's heart after injection of ACPs derived from a human-PBMC-derived CCP, produced in accordance with an embodiment of the present invention;

FIG. 10 is a photograph showing the morphology of cardiomyocytes derived from the CCP and produced in accordance with an embodiment of the present invention;

FIGS. 11A, 11B, and 11C are photographs showing immunostaining of CCP-derived cardiomyocytes, in accordance with an embodiment of the present invention;

FIGS. 12A and 12B are graphs showing flow cytometry analysis results, obtained from immunostaining of a cardiomyocyte-rich PCP, in accordance with an embodiment of the present invention; and

FIG. 13 is a graph showing experimental results of improved ejection fraction in a rat model of acute myocardial infarction following injection of the CCP-derived cardiomyocytes, in accordance with an embodiment of the present invention.

DETAILED DESCRIPTION OF EMBODIMENTS EXAMPLE 1

A test was carried out in accordance with an embodiment of the present invention, and results are shown in Table 1 below. Peripheral blood was extracted from ten human volunteers for use in ten respective experiments. In each experiment, cells were fractioned from the blood using a Ficoll™ gradient in order to generate a population of peripheral blood mononuclear (PBMC) cells as source cells (“S. cells”). Subsequently, a CCP was generated in accordance with protocols described herein for Percoll (TM) based enrichment. Results in Table 1 show enrichment of the percentages of CD34+CD45−/Dim cells in the CCP compared to the source cells. Enrichment is defined as the percentage of cells having a given characteristic in the CCP, divided by the percentage of cells having that characteristic in the source cells.

TABLE 1 % CD34+ % Viability % CD45 CD45−/Dim Exp S. S. Enrichment No cells CCP cells CCP S. cells CCP factor 1 97.56 97.86 94.00 93.46 1.4 4.07 2.9 2 98.49 97.61 92.09 87.10 0.77 3.48 4.5 3 94.28 100 94.72 96.44 0.72 2.31 3.2 4 98.82 98.18 93.11 92.77 0.24 2.69 11.2 5 98.10 98.53 63.15 84.30 1.78 2.77 1.6 6 98.54 98.33 91.58 76.16 0.69 2.37 3.4 7 98.18 97.78 95.58 94.46 0.88 3.7 4.2 8 99.49 97.93 96.11 92.39 0.83 6.14 7.4 9 99.09 97.64 96.75 96.55 0.39 2.24 5.7 10  97.53 99.37 84.46 98.44 0.52 1.67 3.2 AVG 98.01 98.32 90.58 91.41 0.82 3.14 4.7

EXAMPLE 2

In a separate set of experiments, in accordance with an embodiment of the present invention, results were obtained as shown in FIG. 1 and Table 2 below. Peripheral blood was extracted from ten human volunteers for use in ten experiments. A CCP was generated in accordance with protocols described herein (see Example 1). Results in FIG. 1 and in Table 2 show the fluorescent intensity of CD31Bright cells in the CCP. CD31 brightness (Dim or Bright) is defined as the ratio between intensity resulting from staining using anti-CD31 FITC-conjugated monoclonal antibodies and intensity resulting from staining using isotype control FITC-conjugated antibodies.

FIG. 1 is a graph showing results obtained from CCP cells in one representative experiment, in accordance with an embodiment of the present invention. CCP cells stained using isotype control FITC-conjugated antibodies are represented by the dashed line and CCP cells stained using FITC-conjugated anti-CD31 antibodies are represented by the black line. Three different intensity areas were marked:

(a) M1—low intensity corresponding to non-specific staining of isotype control or cells that do not express CD31, located at geometric mean intensity of 5.38;

(b) M2—dim intensity corresponding to cells expressing CD31 at a geometric mean intensity of 46.69; and

(c) M3—bright intensity corresponding to cells expressing CD31 at a geometric mean intensity of 478.45.

Table 2 is a numerical summary of intensities M1, M2 and M3 and their respective ratios resulting from ten independent experiments.

TABLE 2 CD31 Intensity Geo Mean Isotype EXP Control dim bright Intensity Ratio No. M1 M2 M3 M2/M1 M3/M1 M3/M2 1 5.25 42.90 299.92 8 57 7 2 5.38 46.69 478.45 9 89 10 3 5.52 30.37 340.24 6 62 11 4 4.9 28.41 266.46 6 54 9 5 4.57 33.19 456.80 7 100 14 6 5.31 34.94 384.76 7 72 11 7 2.91 25.45 318.20 9 109 13 8 2.19 27.43 361.86 13 165 13 9 3.86 33.57 310.46 9 80 9 10  5.3 42.68 400.03 8 75 9 AVG 4.52 34.56 361.72 8.00 86.50 10.69 SE 0.37 2.30 21.74 0.63 10.42 0.66 CD31Bright cells' (M3) mean intensity is 86.5 (SE=10.42) times greater than the negative control intensity (M1) and 10.69 (SE=0.66) times more than CD31Dim cells (M2) (which themselves have an intensity 8.00 (SE=0.63) times more than M1). Thus, results indicate that the CCP was enriched to provide CD31+ cells.

EXAMPLE 3

In a separate set of experiments, in accordance with an embodiment of the present invention, results were obtained as shown in Table 3 below. Peripheral blood was extracted from nine human volunteers for use in nine experiments. A CCP was generated in accordance with protocols described hereinabove with reference to Example 1.

TABLE 3 % CD31Bright Enrichment Exp No. S. Cells CCP Factor 1 10.1 60.4 6.0 2 25.4 80.85 3.2 3 19.1 76.85 4.0 4 25.1 77.3 3.1 5 16.1 75.8 4.7 6 12.7 75.0 5.9 7 17.5 53.3 3.1 8 21.9 80.96 3.7 9 18.6 64.58 3.5 AVG 18.5 71.67 4.13 Results in Table 3 indicate percentage enrichment of CD31Bright cells in the CCP as compared to the source cells.

EXAMPLE 4

In a separate set of experiments, a human-PBMC-derived CCP was cultured in order to generate an ACP-rich PCP; the CCP was grown on fibronectin or plasma-coated T75 flasks in the presence of medium containing autologous serum (>=10%), 2 ng/ml VEGF, and 5 IU/ml Heparin.

FIG. 2 is a photograph showing the morphology of a typical angiogenic cell precursor (ACP) population, produced in the experiments of Example 3, in accordance with an embodiment of the present invention. Typically, elongated and spindle-shaped cells are observed in cultures of ACPs. This image was obtained from ×200 magnification of cultured ACPs.

EXAMPLE 5

In a separate set of experiments, a human-PBMC-derived CCP was cultured in order to generate an ACP-rich PCP, as described hereinabove with respect to Example 4. The CCP was grown on fibronectin or plasma-coated T75 flasks in the presence of medium containing autologous serum (>=10%), 2 ng/ml VEGF, and 5 IU/ml Heparin.

FIG. 3 contains photographs of a typical angiogenic cell precursor (ACP) population, produced in the experiments of Example 2, in accordance with an embodiment of the present invention. Harvested cells were loaded on a glass slide and fixed prior to their specific staining. Stained cells were mounted using a fluorescent mounting solution containing the nuclear stain DAPI. Figures A1-A3 are a series of photographs from cells stained with FITC-conjugated Ulex-Lectin, cells stained with PE-conjugated anti-CD31, or cells that stained with both Ulex-Lectin and anti-CD31, in accordance with respective embodiments of the present invention. A1 is a photograph of cells stained with the nuclear marker DAPI. A2 is a photograph showing green emission resulting from staining of the same cells with FITC-conjugated Ulex-lectin. A3 is a photograph showing red emission resulting from staining of the same cells with PE-conjugated anti-CD31 antibodies. Figures B1-B3 are a series of photographs from cells stained with isotype control antibodies, in accordance with respective embodiments of the present invention. B1 is a photograph of cells stained with the nuclear marker DAPI, B2 is a photograph showing green emission resulting from staining of the same cells with FITC-conjugated mouse IgG antibodies, and B3 is a photograph showing red emission resulting from staining of the same cells with PE-conjugated mouse IgG Antibodies.

Typically, ACP cells fluoresce both red and green indicating adhesion of both Ulex-Lectin and anti-CD31 thereto. Images were obtained from ×200 magnification.

EXAMPLE 6

In a separate set of experiments, a human-PBMC-derived CCP was cultured in order to generate an ACP-rich PCP, as described hereinabove with reference to Example 4. The CCP was grown on fibronectin or plasma-coated T75 flasks in the presence of medium containing autologous serum (>=10%), 2 ng/ml VEGF, and 5 IU/ml Heparin.

FIG. 4 contains photographs of a typical angiogenic cell precursor (ACP) population, produced in the experiments of Example 4, in accordance with an embodiment of the present invention. Harvested cells were loaded on a glass slide and fixed prior to their specific staining. Stained cells were mounted with a fluorescent mounting solution containing the nuclear stain DAPI. Figures A2-A3 are a series of photographs demonstrating uptake of Ac-LDL, cells stained with anti-CD31, or cells that show both uptake of Ac-LDL and staining with anti-CD31, in accordance with respective embodiments of the present invention. A1 is a photograph of cells stained with the nuclear marker DAN, A2 is a photograph showing green emission resulting from uptake of FITC labeled-Ac-LDL by the same cells, and A3 is a photograph showing red emission resulting from staining of the same cells with PE-conjugated anti-CD31 antibodies. Figures B1-B3 are a series of photographs from cells stained with isotype control antibodies, in accordance with an embodiment of the present invention. B1 is a photograph of cells stained with the nuclear marker DAPI, B2 is a photograph showing green emission resulting from staining of the same cells with FITC-conjugated mouse IgG antibodies, and A3 is a photograph showing red emission resulting from staining of the same cells with PE-conjugated mouse IgG Antibodies.

Typically, ACP cells fluoresce both green and red indicating that ACPs uptake Ac-LDL as well as comprise CD31. Images were obtained from ×200 magnification.

EXAMPLE 7

In the same set of experiments, the human-PBMC-derived CCP was cultured in order to generate an ACP-rich PCP as described hereinabove with respect to Example 4. Flow-cytometry percentage staining results from nine independent experiments are summarized in Table 4, and show the average staining results obtained on day 5 of culturing.

TABLE 4 Number experiments Average on Standard (n) day 5 Error % CD34 9 53.1 6.9 % KDR 9 2.3 1.1 % Tie-2 9 6.6 1.6 % Ac-LDL x CD31Bright 9 60.7 4.7 Results using such a protocol typically yield a PCP having an average of 60.7% of cells that both demonstrate uptake of Ac-LDL and stain for CD31Bright.

EXAMPLE 8

In a separate set of experiments, a human-PBMC-derived CCP was cultured in order to generate an ACP-rich PCP, as described hereinabove with respect to Example 4. Harvested ACP-rich PCP cells were washed from culture medium and incubated for 24 hours in a serum-free medium. Average secretion levels (pg/ml) of IL-8, VEGF, and angiogenin as obtained from four independent experiments are summarized in Table 5.

TABLE 5 Group IL-8 pg/ml VEGF pg/ml Angiogenin pg/ml Control Medium ≦20 ≦20 ≦20 ACP derived 10107 165 615 medium

EXAMPLE 9

In the same set of experiments, a human-PBMC-derived CCP was cultured in order to generate an ACP-rich PCP, as described hereinabove with reference to Example 4. Angiogenic pattern and vascular tube formation of ACP-rich PCP cells were examined microscopically following plating of the cells on an extracellular matrix gel (ECM). Typically, semi-closed and closed polygons of capillaries and complex mesh-like capillary structures were observed and scored according to a scale published by Kayisli et al. (52) as grade 4-5, indicating the angiogenic-inducing properties of the ACP-rich PCP.

FIG. 5 is a photograph showing tube formation in an ACPs, produced in the experiments of Example 6, in accordance with an embodiment of the present invention. Typical mesh-like capillary structures generated from a harvested ACPs are present in the culture and are suitable for administration to a human.

EXAMPLE 10

In a separate set of experiments, a human-PBMC-derived CCP was cultured in order to generate an ACP-rich PCP; the CCP was grown on fibronectin or plasma-coated T75 flasks in the presence of medium containing autologous serum (>=10%), 2-10 ng/ml VEGF, and 5 IU/ml Heparin. At the end of the culturing period, ACP cells were harvested and labeled with 0.8 ug/ml Ac-LDL-DiO for 15 min at 37 C and placed in inserts which were placed in wells. One million labeled ACPs were placed on microporous membrane inserts with a pore size of 8 micrometer. 200 ul medium was placed at the bottom of each of the wells. Negative control (M199), positive control (e.g., 20 ng/ml VEGF, 20 ng/ml bFGF, and 20 ng/ml SCF) and 0.08-60 ng/ml human recombinant Interleukin-8 (hIL-8) diluted in M199 medium were plated in respective wells and the ACP cells were allowed to migrate toward each respective medium. Following 1 hour incubation in the presence of the negative control medium, the positive control medium, and the IL-8 containing media, labeled migrating cells from 10-15 random microscopic fields were evaluated using fluorescent microscope and automated counting software (NTH ImageJ). Calculation of cell number per 1 mm^2 was based on area of counting field (×20) which equals 0.178 mm^2, and each mm^2 contains 5.62 fields. Assessment of ACP migratory potential indicated that ACPs migrate toward chemokines such as VEGF, bFGF, SCF, and hIL-8 in a manner dependent on respective concentrations thereof, e.g., hIL-8 concentration of typically higher than 6.7 ng/ml induces substantial migration of ACPs, and hIL-8 concentrations of about 7-20 ng/ml typically induce substantial migration of ACPs.

FIGS. 6A and 6B are graphs showing results obtained in five experiments of Example 10, in accordance with an embodiment of the present invention. FIG. 6A shows migration toward negative and positive control media of Ac-LDL-DiO pre-labeled ACPs. FIG. 6B shows a dosage-dependence curve reflecting migration of Ac-LDL-DiO pre-labeled ACPs in response to increasing concentrations of hIL-8. ACPs derived from the human-PBMC-derived CCP show statistically significant migration toward the positive control samples. Moreover, ACP migration corresponding to increasing hIL-8 doses was observed. Dose-dependent ACP migration peaked at 6.7-20 ng/ml of hIL-8.

EXAMPLE 11

In a separate set of experiments, the human-PBMC-derived CCP was cultured in order to generate an ACP-rich PCP, as described hereinabove with reference to Examples 4 or 10. In some embodiments, generation of the ACP-rich PCP is attributed to migration of ACP cells to a specific chemokine, in combination with the differentiation of CCP cells. Migratory potential of ACP-rich PCP was measured as described hereinabove with respect to Example 10. In this example, a conditioned medium (CM) was generated using the patients' cells which secrete chemokines into the medium. The patients' cells were then extracted from the medium, leaving a chemokine-rich medium for subsequent plating of ACP therein. The potential for

ACP migration in response to chemokines was then assessed when the ACPs were incubated for 1 hour with conditioned medium.

Following 1 hour incubation in the presence of negative control (M199); 20 ng/ml hIL-8; or CM (at concentrations of 2-20 ng/ml), migration of labeled cells from 10-15 random microscopic fields was evaluated using a fluorescent microscope and automated counting software (NIH ImageJ). Calculation of cell number per 1 mm^2 is based on area of counting field (×20)=0.148 mm^2 and thus each square millimeter contains 6.7 fields. It was determined that ACPs migrate toward chemokines secreted during the production of the ACP-rich PCP.

For some applications, the generated ACP-rich PCP batches were used to treat cardiovascular patients. All patients treated with these batches showed more than 10% improvement in left-ventricular-ejection fraction both 3 and 6 months following treatment. It is hypothesized that this improvement was enabled at least in part by the migration of ACPs to the vicinity.

FIG. 7 is a graph showing results obtained in four experiments of Example 11, in accordance with an embodiment of the present invention. The ACPs derived from the human-PBMC-derived CCP show statistically significant migration toward the conditioned medium containing secreted chemokines; this medium was generated in the process of the production of ACP-rich PCP.

EXAMPLE 12

In a separate set of experiments, migratory potential of human-PBMC toward hIL-8 was measured. In vitro assessment of PBMC migratory capability in response to hIL-8 was used to determine the potential of IL-8 to mobilize blood derived stem/progenitor cells from peripheral blood to locations in which high concentrations of IL-8 are expressed in vivo. Peripheral blood was extracted from six human volunteers for use in six respective experiments. In each experiment, a Ficoll™ gradient was used to generate a population of PBMCs. One million PBMCs were placed on 3 um pore size microporous membrane inserts which were placed in wells. 200 ul medium was placed at the bottom of each of the wells. Negative control (M199) and positive control (20 ng/ml hIL-8) diluted in M199 medium were plated in respective wells and the PBMCs cells were allowed to migrate toward each respective medium. Following 1 hour incubation in the presence of the negative control medium and the positive control medium, migration of cells from 10-15 random microscopic fields was evaluated using a fluorescent microscope and automated counting software (NIH ImageJ). Calculation of cell number per 1 mm^2 is based on area of counting field (×20) which equals 0.148 mm^2, and each square millimeter contains 6.7 fields. It was determined that hIL-8 induced mobilization of only a small fraction of the PBMCs, probably the stem/progenitor cells.

FIG. 8 is a graph of migration of PBMCs in response to hIL-8, in accordance with an embodiment of the present invention. The results were obtained from six experiments (Example 12), and show that stem/progenitor cells derived from human-PBMCs migrate toward hIL-8.

EXAMPLE 13

Reference is now made to FIGS. 9A and 9B which are graphs showing results obtained in the experiments following injection into rats of ACP-rich PCPs derived from a human-PBMC-derived CCP (as described hereinabove with respect to Example 4) following acute myocardial infarction, in accordance with an embodiment of the present invention.

The human-PBMC-derived CCP was cultured in order to generate an ACP-rich PCP as described in Example 4. ACP-rich PCP therapeutic potential was then assessed in a rat model of acute myocardial infarction which was induced in 15 male nude rats (200-225 g) by ligation of the left anterior descending (LAD) artery. Six days after myocardial infarction, 10 rats were injected with 1.5×10^6 ACP-enriched cells (ACP, n=10), while 5 rats were injected with the culture medium (Control, n=5), via the aortic arch. Cardiac function (ejection fraction) and the ratio of necrotic scar area to left ventricular free wall area were measured 28 days following the ACP-rich PCP and the culture medium administrations. It is to be noted that the percentage of ejection fraction of the ACP-administered rats, as represented by FIG. 9A, increased substantially in comparison to the decreased percentage ejection fraction of the control rats. Additionally, a percentage reduction of necrotic tissue was observed in the ACP-administered rats in comparison to the percentage of necrotic tissue observed in the control rats. Paraffin fixed tissue sections obtained from the 10 ACP-administered rats were stained in order to trace engrafted human cells and cardiomyocyte (CMC) markers in the border area of the scar tissue.

FIGS. 9C, 9D and 9E are photographs showing typical sections taken from a heart of one of the 10 rats 28 days after the injection of the ACPs derived from a human-PBMC-derived CCP in the experiments of the present example (Example 13) in accordance with an embodiment of the present invention. FIG. 9C shows staining of the rat's heart cells with anti-human mitochondria. FIG. 9D shows the cells stained for CMC markers (myosin heavy chain (MHC)), FIG. 9E shows the rat heart cells stained for cardiac Troponin I. (Reference is again made to FIG. 9C-E. The stained cells are marked by arrows). These results depicted in FIGS. 9C-D demonstrate that the human ACPs, derived in accordance with an embodiment of the present invention from the hPBMC-derived CCP, homed to damaged cardiac tissues, engrafted, and is hypothesized to have transdifferentiated into cells expressing cardiomyocyte markers.

It is to be noted that ACPs typically improve systemic endothelial functioning, as expressed by improved ejection fraction and reduced necrosis. Particular examples of improvement due to administration of ACPs, derived in accordance with an embodiment of the present invention, include improved cardiovascular functioning and improved sexual functioning. The scope of the present invention includes identifying a patient having cardiovascular dysfunction or sexual dysfunction, and administering ACPs to the patient in order to treat the dysfunction.

EXAMPLE 14

In a production procedure, individual autologous human-PBMC-derived CCPs were cultured in order to generate an ACP-rich PCP, as described hereinabove. The CCPs were grown on autologous plasma-coated T75 flasks in the presence of medium containing autologous serum (>=10%), 2-10 ng/ml VEGF, and 5 IU/ml Heparin. Harvested cells, approved by Quality Control for clinical use, were administrated to patients. The therapeutic potential of ACP-rich PCP is summarized in results of administration thereof to 14 patients suffering from end-stage heart failure. Left ventricular ejection fraction (EF) and disease severity score (Score) were assessed prior to and 1-8 months after the ACP cell administration. Improvement of these parameters was calculated relative to each patient's baseline evaluation according to the following equation: % Improvement=(Test result after treatment−Baseline test result)/Baseline test result.

Results show statistically significant improvement (p<0.0001; tested using two-tailed, paired t test analysis) in both parameters following treatment by administering ACP-rich PCP.

Table 6 shows the number of treated patients, averages and individual results relating to EF and disease severity score, as well as the calculated percent improvement thereof.

TABLE 6 % EF* SCORE* % EF At 1-8 EF % SCORE At 1-8 SCORE % Batch No. Baseline Months Improvement Baseline Months Improvement N 14 14 14 14.0 14.0 14.0 Average 24.1 34.8 49.8 2.9 1.6 45.6 Range 14.9-36.0 20.0-50.0 11.1-133 2.0-4.0 1.0-3.0 29.0-67.0 SE 2.1 2.8 10.9 0.1 0.1 4.1 PCEPC066 30.0 40.0 33.3 2.00 1.00 50.00 PCEPC081 23.0 50.0 117.4 3.00 1.00 66.67 PCEPC083 27.5 32.5 18.2 3.00 2.00 33.33 PCEPC091 14.9 20.0 34.2 3.00 2.00 33.33 PCEPC092 35.0 41.0 17.1 3.00 2.00 33.33 PCEPC094 36.0 40.0 11.1 3.00 2.00 33.33 PCEPC097 15.0 27.5 83.3 3.00 1.00 66.67 PCEPC099 15.0 35.0 133.3 3.50 2.00 42.86 PCEPC103 18.3 20.9 14.2 3.00 2.00 33.33 PCEPC106 15.0 20.0 33.3 3.00 1.00 66.67 PCEPC110 25.0 50.0 100.0 3.00 2.00 33.33 PCEPC114 22.0 30.0 36.4 2.00 1.00 50.00 PCEPC121 25.0 32.0 28.0 3.50 2.50 28.57 PCEPC137 35.0 48.0 37.1 3.00 1.00 66.67 *Significant improvement p < 0.0001

EXAMPLE 15

In a separate set of experiments, a human-PBMC-derived CCP was cultured in order to generate a cardiomyocyte (CMC)-rich PCP; the CCP was grown on fibronectin or plasma-coated T75 flasks in accordance with protocols described herein (see medium preparation).

FIG. 10 is a photograph of a typical CMC-rich PCP from the experiments of the current example (Example 15), derived in accordance with an embodiment of the present invention. Typically, these cells appear elongated with dark cytoplasm, which may indicate high protein content. This image was obtained from ×200 magnification of cultured CMC-rich PCP cells.

FIGS. 11A, 11B, and 11C are photographs showing immunostaining of CCP-derived cardiomyocytes in the experiments of the current example (Example 15), in accordance with an embodiment of the present invention. Slide-fixed CMC PCP cells were stained with:

FIG. 11A—anti-cardiac Troponin detected by anti-mouse Cy-3;

FIG. 11B—anti-alpha-actin detected by anti-mouse IgG-FITC; and

FIG. 11C—anti-connexin 43 detected by anti-mouse IgG-FITC.

Cells stained with non-specific mouse IgG were detected by anti-mouse IgG-FITC or by anti-mouse IgG-Cy3 and were used as negative controls.

FIGS. 11A-C show that CMC-rich PCP cells expressed the typical cardiomyocyte cellular markers: cardiac Troponin T (FIG. 11A), alpha-actin (FIG. 11B), as well as the functionally important GAP junction marker connexin-43 (FIG. 11C). The images were obtained from ×100 magnification of slide-fixed cells.

EXAMPLE 16

In the same set of experiments that produced the results shown in FIGS. 10-11C, a human-PBMC-derived CCP was cultured in order to generate a CMC-rich PCP; the CCP was grown on fibronectin or plasma-coated T75 flasks in accordance with protocols described herein (see medium preparation).

FIGS. 12A and 12B are graphs showing flow cytometry analysis results obtained from immunostaining of a CMC-rich PCP in the experiments of the current example (Example 16), in accordance with respective embodiments of the present invention. In FIGS. 12A-B, lines describing control, e.g., non-specific staining, are marked as “Control”; specific immunostaining with the cardiac cellular markers desmin and troponin T are marked as Desmin (FIG. 12A) and Troponin T (FIG. 12B), respectively. The M1 line represents the statistical marker area in which the cells are positively stained for the respective marker.

EXAMPLE 17

In a separate set of experiments, a human-PBMC-derived CCP was cultured in order to generate a CMC-rich PCP, as described hereinabove. The CMC-rich PCP cells' therapeutic potential was assessed in a rat model of acute myocardial infarction. CMC-rich PCP cells were used for implantation into a rat model of induced acute myocardial infarction as described hereinabove with respect to Example 13 (with the exception that CMC-rich PCP cells were used for implantation into the rat model in the current example, whereas in Example 13, ACP-rich PCP cells were used for implantation). Six days after myocardial infarction, heart muscle of 9 rats were injected with 1.5×10^6 CMC PCP cells (CMC, n=9), while heart muscle of 5 rats were injected with culture medium (Control, n=5). Cardiac function (ejection fraction) was evaluated 14 days following the administration of the CMC-rich PCP cells or culture medium.

FIG. 13 is a graph showing experimental results obtained in the experiments of Example 13, in accordance with another embodiment of the present invention. It is to be noted that the percentage of ejection fraction of the CMC-administered rats increased substantially in comparison to the decreased percentage ejection fraction of the control rats.

A series of protocols are described hereinbelow which may be used, as appropriate, separately or in combination with Examples 1-17, in accordance with embodiments of the present invention. It is to be appreciated that numerical values are provided by way of illustration and not limitation. Typically, but not necessarily, protocols may be derived using values selected from a range of values that is within 20% of the value shown. Similarly, although certain steps are described herein with a high level of specificity, a person of ordinary skill in the art will appreciate that additional or other steps may be performed, mutatis mutandis.

In accordance with an embodiment of the present invention; generation of a single-cell suspension is carried out using the following protocols:

Protocol 1: Extraction of Peripheral Blood Mononuclear Cells (PBMC).

-   -   Receive blood bag and sterilize it with 70% alcohol. Load blood         cells onto a Ficoll™ gradient.     -   Spin the tubes for 20 minutes at 1050 g at room temperature         (RT), with no brake.     -   Collect most of the plasma from the supernatant.     -   Collect the white blood cell fraction from every tube.     -   Transfer the collected cells to a new 50 ml tube, adjust volume         to 30 ml per tube using PBS.     -   Spin tubes for 15 minutes at 580 g, RT, and discard supernatant.     -   Count cells in Trypan Blue.     -   Re-suspend in culture medium comprising, for example, X-vivo         15™.         Protocol 2: Extraction of Cells from Umbilical Cord.     -   Isolate 10 cm umbilical cord.     -   Wash thoroughly with sterile PBS.     -   Identify the major vein of the cord, and clamp one end of the         vein.     -   Wash twice with 30 ml sterile PBS.     -   Fill vein with 0.15% collagenase (about 5 ml of 0.15%         collagenase solution).     -   Clamp the second end of the vein.     -   Incubate at 37 C for 15 min.     -   Wash outer side of the cord with 70% ethanol.     -   Release the clamp from one end of the vein and collect the cell         suspension.     -   Centrifuge for 10 min at 580 g, 21 C.     -   Re-suspend the cells in culture medium comprising, for example,         X-vivo 15™, 10% autologous serum, 5 IU/ml heparin, and one or         more growth factors.         Protocol 3: Extraction of Cells from Bone Marrow.     -   Get bone marrow aspiration from surgical room.     -   Re-suspend in culture medium comprising, for example, X-vivo         15™, 10% autologous serum, 5 IU/ml heparin, and one or more         growth factors.     -   Pass suspension through a 200 um mesh.

In accordance with an embodiment of the present invention, generation of a CCP is carried out using the following protocols:

Protocol 1: Generation of a Human CCP from PBMCs Using a Percoll™ Gradient.

-   -   Prepare gradient by mixing a ratio of 5.55 Percoll™ (1.13 g/ml):         3.6 ddH2O: 1 PBSx10.     -   For every 50 ml tube of Percoll: mix 20 ml of Percoll™ stock, 13         ml of ddH2O and 3.6 ml of PBSx10.     -   Mix vigorously, by vortexing, for at least 1 min.     -   Load 34 ml mix into each 50 ml tube.     -   Centrifuge tubes, in a fixed angle rotor, for 30 min at 17,000         g, 21 C, with no brake.     -   Gently layer 3.0 ml of cell suspension of 150 million-400         million PBMCs on top of the gradient.     -   Prepare a second tube with density marker beads: gently layer         3.0 ml of medium on top of the gradient.     -   Gently load density marker beads—10 ul from each bead type.

Centrifuge tubes, in a swinging bucket rotor, for 30 min at 1260 g at 13 C, with no brake.

-   -   Gently collect all bands located above the red beads, and         transfer to tube with 10 ml medium.     -   Centrifuge cells for 15 min at 580 g at 21 C.     -   Discard supernatant and re-suspend pellet in medium.     -   Count cells in Trypan blue.     -   Centrifuge cells for 10 min at 390 g, 21 C.     -   Discard supernatant and re-suspend pellet in medium.     -   Take CCP cells for FACS staining.         Protocol 2: Generation of Human CCP from PBMCs Using an         OptiPrep™ Gradient.     -   Take up to 130 million cells for each enrichment tube.     -   Spin cells for 10 min at 394 g, 21 C.     -   Suspend cell pellet in 10 ml of donor serum.     -   Prepare a 1.068 g/ml OptiPrep™ gradient by mixing a ratio of 1         OptiPrep™: 4.1 PBS.     -   For every 50 ml enrichment tube:     -   Mix 10 ml of cell suspension with 4 ml OptiPrep™.     -   For preparation of a 1.068 g/ml OptiPrep™ gradient, mix 5 ml of         OptiPrep™ and 20.5 ml of PBS.     -   Gently layer 20 ml of the 1.068 g/ml gradient on top of the cell         suspension.     -   Gently layer 1.5 ml Hank's buffered saline (HBS) on top of the         gradient layer.     -   Centrifuge for 30 min at 700 g at 4 C, with no brake.     -   Gently collect the layer of cells that floats to the top of the         1.068 g/ml OptiPrep™ gradient into a 50 ml tube pre-filled with         PBS.     -   Centrifuge for 10 min at 394 g, 21 C.     -   Discard supernatant and re-suspend pellet in medium.     -   Count cells in Trypan Blue.

It is to be noted that culture containers are typically either un-coated or coated with one or a combination of ACP-enhancing materials such as collagen, fibronectin, CD34, CD133, Tie-2, or anti-CD117.

In accordance with an embodiment of the present invention, the coating of a tissue culture container is carried out using the following protocols:

Protocol 1: Coating T75 Glasks with 25 ug/ml Fibronectin.

For 20 T75 flasks—Prepare up to seven days before, or on day of PBMC preparation.

Prepare 50 ml of 25 ug/ml fibronectin solution in PBS.

Fill every flask with 2-5 ml fibronectin 25 ug/ml.

Incubate at 37 C for at least 30 min.

Collect fibronectin solution.

Wash flask twice in PBS.

Dry flasks

Keep dry flasks at room temperature.

Dried flasks can be saved for one week at room temperature (RT).

Protocol 2: Coating T75 Flasks with 25 ug/ml Fibronectin and 5 ng/ml BDNF

Coat flasks with Fibronectin 25 μg/ml, as described in Protocol 1.

Prepare 50 ml of 5 ng/ml BDNF solution in PBS.

After washing off Fibronectin, fill every flask with 2-5 ml BDNF 10 ng/ml.

Incubate at 37 C for 1 hour.

Collect the solution.

Wash flask twice in 10 ml PBS.

Keep dry flasks at room temperature until use.

In accordance with an embodiment of the present invention, serum preparation is carried out using the following protocol: (Serum can be obtained directly or prepared from plasma).

Protocol: Preparation of serum from human plasma.

Take 100 ml of undiluted blood.

Spin at 1100 g (2500 rpm) for 10 min.

Transfer the upper layer (plasma) to a new 50 ml tube.

Add 1.0 ml 0.8M CaCl₂-2H₂O for every 40 ml plasma.

Incubate for 0.5-3 hours at 37 C.

Spin coagulated plasma 5 min at 2500 g.

Collect the serum in a new tube, avoiding clotting.

Aliquot collected serum and save at −20 C until use.

In accordance with an embodiment of the present invention, medium preparation is carried out using the following protocols:

Medium should contain 1-20% autologous serum and/or 1-20% conditioned medium.

Medium can contain one or more additives, such as LIF, EPO, IGF, b-FGF, M-CSF, GM-CSF, TGF alpha, TGF beta, VEGF, BHA, BDNF, NGF, EGF, NT3, NT4/5, GDNF, S-100, CNTF, NGF3, CFN, ADMIF, estrogen, progesterone, cortisone, cortisol, dexamethasone, or any other molecule from the steroid family, prolactin, an adrenocorticoid hormone, ACTH, glutamate, serotonin, acetylcholine, NO, retinoic acid (RA) or any other vitamin D derivative, Heparin, insulin, forskolin, Simvastatin, MCDB-201, MCT-165, glatiramer acetate, a glatiramer acetate-like molecule, IFN alpha, IFN beta or any other immunoregulatory agent sodium selenite, linoleic acid, ascorbic acid, transferrin, 5-azacytidine, PDGF, VEGF, cardiotrophin, and thrombin or Rosiglitazone in various concentrations, typically ranging from about 100 pg/ml to about 100 μg/ml (or molar equivalents).

Typically, medium should not be used more than 10 days from its preparation date.

Protocol 1: Medium for Enhancement of CCP-Derived Angiogenic Cell Precursors (ACPs).

Serum-free medium (e.g., X-vivo 15™)

10% autologous serum

5 IU/ml Heparin

5 ng/ml VEGF

1 ng/ml EPO

Protocol 2: Medium for Enhancement of CCP-Derived Neuronal Progenitor Cells.

Serum-free medium (e.g., X-vivo 15™)

20 ng/ml bFGF

50 ng/ml NGF

200 uM BHA (this is added during the last 24 hours of culturing)

10 ng/ml IFN beta

10 ug/ml glatiramer acetate

10 uM forskolin

1 uM cortisone

1 ug/ml insulin

Protocol 2.1: Medium for Enhancement of CCP-Derived Neuronal Progenitor Cells.

Serum-free medium (e.g., X-vivo 15™)

20 ng/ml bFGF

50 ng/ml NGF

25 ng/ml BDNF

200 uM BHA (this is added during the last 24 hours of culturing)

Protocol 3: Medium for Enhancement of CCP-Derived Retinal Cells.

Serum-free medium (e.g., X-vivo 15™)

10% autologous serum

5 IU/ml Heparin

10 ng/ml EGF

20 ng/ml bFGF

10 ug/ml glatiramer acetate

50 ng/ml NGF3

Protocol 4a. Medium for Enhancement of CCP-Derived Cardiomyocyte (CMC) Progenitor Cells.

Step I

Serum-free medium (e.g., X-vivo 15™)

10% autologous serum

20 ng/ml bFGF

20 ug/ml IFN beta

5 IU heparin.

Step II

Five to ten days after culture onset, add 3 uM 5-azacytidine for 24 hours.

Protocol 4b: Medium for Enhancement of CCP-Derived CMC Progenitor Cells.

Serum free medium DMEM-Low glucose

20% autologous serum

10% MCDB-201

2 ug/ml Insulin

2 ug/ml Transferin

10 ng/ml Sodium Selenite

50 mg/ml BSA

1 nM Dexamethasone

20 ug/ml Glatiramer acetate

0.47 ug/ml Linoleic acid

0.1 mM Ascorbic Acid

100 U/ml penicillin

In accordance with an embodiment of the present invention, conditioned medium preparation is carried out using the following protocol:

Protocol 1: Preparation of 100 ml Enriched Medium Containing 10% Autologous Conditioned Medium.

Thaw 10 ml conditioned medium in an incubator.

When thawed, add it to culture medium using pipette.

Extraction of Tissue Pieces for Co-Culture:

Dissection of rat blood vessels (other non-human or human tissues may also be used):

-   -   Anesthetize animal using anesthetic reagents (e.g., 60-70% CO2,         isoflurane, benzocaine, etc.).     -   Lay animal on its back and fix it to an operating table.     -   Using sterile scissors, cut animal's skin and expose the inner         dermis.     -   Using a second set of sterile scissors, cut the dermis, cut         chest bones, and expose the heart and aorta.     -   Cut small pieces, 0.2-1 cm long, from the aorta and other blood         vessels, and place them in a container pre-filled with 50 ml         cold culture medium (e.g. RPMI, X-vivo 15™), or any other growth         medium).     -   Using forceps and scissors, clean tissue sections, to remove         outer layers such as muscle, fat, and connective tissue.     -   Using forceps and scalpel, cut each blood vessel along its         length, and expose the inner layer of endothelial cells.     -   Using forceps and scalpel, cut small pieces of up to 0.1 cm2         from the tissue.

It is to be understood that whereas this technique is in accordance with one embodiment of the present invention, the scope of the present invention includes extracting a blood vessel from a human, as well. For example, an incision may be made over the saphenous vein, in order to facilitate dissection of a distal 1 cm portion of the vein. Tributary veins thereto are tied and transected. Distal and proximal ends of the 1 cm portion of the saphenous vein are tied, and the vein is harvested.

Use the dissected tissue for direct and/or indirect co-culturing with the CCP and/or to generate conditioned medium.

Generation of Conditioned Medium:

-   -   Lay dissected pieces in culture containers, for example in T75         flasks, or 50 ml tubes.     -   Optionally, fill with cell culture medium containing 0.1-3 ug/ml         or 3-100 ug/ml apoptotic reagent (such as valinomycin, etoposide         or Staurosporine), until all pieces are covered.     -   Refresh culture medium every 2 days.     -   Collect this medium (now conditioned medium) into 50 ml tubes.     -   Spin collected conditioned medium at 450 g for 10 min, at room         temperature.     -   Collect supernatant in a new sterile container.

Details regarding preservation of the conditioned medium, in accordance with an embodiment of the present invention, are described hereinbelow.

In accordance with an embodiment of the present invention, culturing of a CCP to produce a PCP is carried out using the following protocols:

Protocol 1: Culturing of CCP Cell Suspension in T75 Flasks.

-   -   Spin suspension for 15 minutes at 450 g, 21 C.     -   Discard the supernatant.     -   Gently, mix cell pellet and re-suspend the CCP cells.     -   Re-suspend pellet to 10 million CCP cells/ml.     -   Fill T75 flask with 15 ml enriched medium, and add 5 ml of 10         million CCP cells/ml to attain a final concentration of 50         million CCP cells/flask.     -   Incubate T75 flasks, plates and slides at 37 C, 5% CO2.         Protocol 2: Applied Hypoxia.

For some applications, increased expansion and/or differentiation of the CCP may be obtained by exposure of the cell culture to oxygen starvation, e.g., 0.1-5% or 5-15% oxygen (hypoxia), for 2-12 or 12-48 hours. This is typically done one or more times, at different points during cell culturing.

Incubate T75 flasks in an oxygen-controlled incubator.

Set the oxygen pressure at 0.1%, and maintain it at this level for 24 hours.

Remove the flasks from the incubator and examine the culture.

Take a sample of CCP cells and test viability by Trypan blue exclusion method.

Set the oxygen pressure of the incubator at 20%.

-   -   Re-insert the flasks into the incubator and continue incubation         for the rest of the period. This procedure can be repeated, for         example, once a week during the culture period and/or within 24,         48, or 72 hours before termination of the culture.         Protocol 3: Reseeding of Adherent and/or Detached and/or         Floating Cells.

For some applications, increased expansion and differentiation of the CCP may be achieved by re-seeding collected cells on new pre-coated dishes in culture medium.

-   -   Collect all cultured CCP in tubes.     -   Spin tubes for 10 minutes at 450 g, 21 C.     -   Discard the supernatant.     -   Gently mix pellet and re-suspend cells in 10 ml fresh medium per         T75 flask.     -   Seed suspended cells in new pre-coated T75 flasks.     -   Continue culturing the cells, and perform all other activities         (e.g., medium refreshment, visual inspection, and/or flow         cytometry), as appropriate, as described herein.

This procedure can be performed weekly during the culture period and/or within 24, 48, or 72 hours before termination of the culture.

In accordance with an embodiment of the present invention, co-culturing of

CCP with tissue-derived conditioned medium is carried out using the following protocol:

Protocol 1: Culturing of CCP in the Presence of Conditioned Medium Derived from a Blood Vessel Culture.

-   -   Spin CCP cells for 15 minutes at 500 g, 21 C.     -   Discard the supernatant.     -   Gently mix cell pellet and re-suspend cells to 5-50 million/ml         in autologous medium containing 1-20% autologous serum and/or         1-20% conditioned medium.     -   Seed flasks with 2-5 million CCP cells/ml.     -   Incubate flasks at 37 C, 5% CO2.     -   After first three days of culture, non-adherent cells can be         removed from the culture.

In accordance with an embodiment of the present invention, refreshing of the media in ongoing growing CCP cultures is carried out using the following protocol:

Refreshing of the media in ongoing growing flasks should occur every 3-4 days.

Protocol 1: Refreshing of Medium in T-75 Flasks.

-   -   Collect non-adherent cells in 50 ml tubes.     -   Fill every flask with 10 ml fresh culture medium enriched with         conditioned medium.     -   Spin tubes for 10 minutes at 450 g, RT; discard the supernatant.     -   Gently mix cell pellet and re-suspend cells in 10 ml/flask fresh         culture medium enriched with condition medium.     -   Return 5 ml of cell suspension to every flask.

In accordance with an embodiment of the present invention, indirect co-culture of CCP cells with tissue dissection is carried out using the following protocol:

Protocol 1: Indirect Co-Culture of Dissected Blood Vessel and CCP Cells in a Semi-Permeable Membrane Apparatus.

-   -   Lay dissected tissue pieces in the upper chamber of the         apparatus on top of the semi-permeable membrane.     -   Implant CCP cells in lower chamber.     -   Lower chamber can be pre-coated with growth-enhancing molecules         such as collagen, plasma, fibronectin, a growth factor,         tissue-derived extra cellular matrix and an antibody.     -   Refresh culture medium in the upper chamber—aspirate conditioned         medium into 50 ml tubes and add autologous culture medium.     -   Preserve collected conditioned medium at −20 C.     -   Remove upper chamber after four days of co-culture.     -   Refresh culture medium of the CCP cells with culture medium         containing 1-20% autologous serum and/or 1-20% conditioned         medium.     -   Continue growing and harvesting as described herein.     -   Co-culture in separate chambers within a culture container

In accordance with an embodiment of the present invention, co-culturing within a culture container is carried out using the following protocol:

Protocol 1: Direct Co-Culturing of Autologous Dissected Blood Vessel and CCP Cells.

-   -   Lay dissected tissue pieces in pre-coated flasks.     -   Implant CCP cells in pre coated second chamber.     -   Using forceps, take out tissue pieces after four days of         co-culture.     -   Refresh culture medium of the CCP cells with culture medium         containing 1-20% autologous serum and/or 1-20% condition medium.     -   Continue growing and harvesting as described herein.

In accordance with an embodiment of the present invention, harvesting of the cellular product is carried out using the following protocol:

Protocol 1: Collection of Resulting ACP Cultures.

-   -   Collect cells in 50 ml tubes.     -   Carefully wash flask surface by pipetting with cold PBS to         detach adherent cells.     -   Collect washed adherent cells to 50 ml tubes.     -   Add 5 ml of cold PBS.     -   Detach remaining adherent cells using gentle movements with cell         scraper.     -   Collect the detached cells and add them to the tubes     -   Optionally, add 5 ml EDTA to each flask and incubate at 37 C for         5 min.     -   Collect the detached cells and add them to the tubes Spin tubes         for 5 min, at 450 g, room temperature.     -   Re-suspend the pellets in 2-5 ml PBS.     -   Count the cells in Trypan blue.

In accordance with an embodiment of the present invention, cellular product preservation is carried out using the following protocols:

Cellular product can be kept in preservation media or frozen in freezing buffer until use for transplantation into a patient.

Protocol 1: Cryopreservation of Cellular Product.

-   -   Prepare freezing buffer containing 90% human autologous serum         and 10% DMSO.     -   Suspend cellular product in freezing buffer and freeze in liquid         nitrogen.         Protocol 2: Short-Period Preservation of Cellular Product.

Prepare preservation medium including growth medium containing 1-20% autologous serum, with few or no other additives. Maintain preservation medium with cellular product at 2-12 C

In accordance with an embodiment of the present invention, conditioned medium collection and preservation is carried out using the following protocol:

-   -   Conditioned medium can be kept until use for growth medium         preparation.     -   Conditioned medium should be collected under sterile conditions.     -   Spin collected conditioned medium for 10 min at 450 g, 21 C.     -   Collect supernatant in a new sterile container.     -   Filter supernatant through a 22 um membrane.     -   Aliquot conditioned medium to 10 and/or 50 ml sterile tubes,         pre-marked with donor details.

Keep at −20 C until use.

In accordance with an embodiment of the present invention, FACS staining is carried out using the following protocol:

Protocol 1: Staining of ACP Enriched Population.

FACS staining protocol:

Tube No. Staining Aim of staining 1. Cells Un-stained control 2. CD45 (IgG1)-FITC Single staining for PMT and 3. CD14-PE (IgG2a) compensation settings 4. CD45 (IgG1)-APC 5. mIgG1-FITC Isotype control mIgG1-PE mIgG1-APC 6. CD45-FITC (IgG1) KDR-PE (IgG2a) CD34-APC (IgG1) 7. Ac-LDL-FITC CD31-PE (IgG1) 8. Ulex-Lectin-FITC CD31-PE (IgG1) 9. mIgG1-FITC Isotype control mIgG2a-PE mIgG1-APC 10. CD45-FITC (IgG1) CD133-PE (IgG2a) CD34-APC (IgG1) Protocol 2: Staining of CMC Progenitors.

FACS staining protocol for fixed permeabilized cells:

Staining Staining Tube No. 1^(st) step 2^(nd) step Aim of staining 1 Cells Un-stained control 2 CD45-FITC (IgG1) Single staining for 3 CD14-PE (IgG2a) PMT and compensation settings 5 mIgG1 Anti mouse-PE Isotype control 6 Desmin Anti mouse-PE 7 Troponin T Anti mouse-PE Isotype control

In accordance with an embodiment of the present invention, immunohistochemistry staining (IHC) is carried out using the following protocols:

Protocol 1: IHC Staining Protocol for ACPs.

Slide Staining No. 1st step Aim of staining 1. mIgG1 Isotype control 2. mIgG1-PE Isotype control 3. CD34-APC Specific Staining 4. CD144-FITC Specific Staining 5. CD133-PE Specific Staining 6. Ac-LDL-FITC Specific Staining CD31-PE 7. Ulex-Lectin-FITC Specific Staining CD31-PE Protocol 2: IHC Staining Protocol for CMC Progenitors.

Slide Staining Staining No. 1st step 2nd step Aim of staining 1. — mIgG1-FITC Isotype control 2. mIgG1 Anti mouse-Cy-3 Isotype control 3. Connexin 43 Anti mouse-FITC Specific Staining 4. Alfa actin Anti mouse-FITC Specific Staining 5. Troponin Anti mouse-PE Specific Staining

In accordance with an embodiment of the present invention, a tube formation assay is carried out using the following protocol:

Tube formation was tested using the ECM625(Chemicon) in vitro angiogenesis assay kit.

Angiogenic pattern and vascular tube formation was numerically scored as described by Kayisli U.A. et al. 2005 (52).

In accordance with an embodiment of the present invention, secretion of cytokines from harvested cells is assessed using the following protocols:

-   -   Culture 0.5-1×10^6 cells/ml over night in 24 well plates in         serum-free medium (e.g., X-vivo 15)     -   Collect culture supernatant and spin at 1400 rpm for 5 minutes     -   Transfer supernatant to an eppendorf tube and freeze at −80 C         until ready to test cytokine secretion.         Protocol 1: ELISA for IL-8.     -   A commercial DuoSet CXCr8/IL-8 (R&D Systems) was used for the         detection of IL-8 secretion.         Protocol 2: Cytometric Bead Array.     -   A commercial cytometric bead array (CBA) kit for human         angiogenesis (BD 558014) was used for the detection of IL-8,         VEGF, TNF and Angiogenin secretion.

It is to be noted that the scope of the present invention includes injecting IL-8 into a human patient in order to recruit ACP cells to a given destination within a given patient, in accordance with the needs of the patient.

For some applications, techniques described herein are practiced in combination with techniques described in one or more of the references cited in the Background section and Cross-References section of the present patent application.

All references cited herein, including patents, patent applications, and articles, are incorporated herein by reference.

It is to be appreciated that by way of illustration and not limitation, techniques are described herein with respect to cells derived from an animal source. The scope of the present invention includes performing the techniques described herein using a CCP derived from non-animal cells (e.g., plant cells), mutatis mutandis.

It will be appreciated by persons skilled in the art that the present invention is not limited to what has been particularly shown and described hereinabove. Rather, the scope of the present invention includes both combinations and subcombinations of the various features described hereinabove, as well as variations and modifications thereof that are not in the prior art, which would occur to persons skilled in the art upon reading the foregoing description. 

The invention claimed is:
 1. A composition of matter, comprising a population of cultured cells that comprises a sub-population of cells that stain as CD31Bright, demonstrate uptake of Ac-LDL+ and secrete interleukin-8 and angiogenin, wherein the sub-population of cells comprises at least 10% of the cells in the population of cultured cells.
 2. The composition of matter according to claim 1, wherein the sub-population secretes at least 50 pg interleukin-8 per 10⁶ cells/ml over a period of at least 24 hours.
 3. The composition of matter according to claim 1, wherein at least 1.5% of the cells of the population comprise a feature selected from the group consisting of: CD34, CD117, CD133, Tie-2, CD34+CD133+, KDR, CD34+KDR+, CD144, von Willebrand Factor, SH2 (CD105), SH3, fibronectin, collagen type I, collagen type III, collagen type IV, ICAM type 1, ICAM type 2, VCAM1, vimentin, BMP-R IA, BMP-RII, CD44, integrin b1, aSM-actin, MUC18, CXCR4 and CXCR8.
 4. The composition of matter according to claim 1, wherein at least 1.5% of the cells of the population secrete a molecule selected from the group consisting of: vascular endothelial growth factor, matrix metalloproteinase-2, and matrix metalloproteinase-9.
 5. The composition of matter according to claim 1, wherein at least 1.5% of the cells of the population include a feature selected from the group consisting of: a tube-like structure, a tendency to form a colony, a tendency to form a cluster, and a tendency to migrate toward a chemoattractant.
 6. The composition of matter according to claim 1, wherein the sub-population comprises at least 25% of the cells in the population.
 7. The composition of matter according to claim 1, wherein the sub-population comprises at least 50% of the cells in the population.
 8. The composition of matter according to claim 1, wherein the sub-population secretes at least 150 pg IL-8 per 10⁶ cells/ml over a period of at least 24 hours.
 9. The composition of matter according to claim 1, wherein the sub-population secretes at least 1000 pg IL-8 per 10⁶ cells/ml over a period of at least 24 hours.
 10. The composition of matter according to claim 1, wherein at least 1.5% of the cells of the population include a morphological feature selected from the group consisting of: a cell size larger than 20 μm, an elongated cell, a spindle-shaped cell, an irregularly-shaped cell, a granulated cell, a cell including an enlarged dark nucleus, a multinuclear cell, a cell including flagella-like structures, a cell including pseudopodia, and a cell having a polygonal shape.
 11. The composition of matter according to claim 1, wherein at least 1.5% of the cells of the population have a tendency to migrate toward a chemoattractant selected from the group consisting of: bFGF, VEGF, SCF, G-CSF, GM-CSF, and SDF-1.
 12. The composition of matter according to claim 1, wherein at least 1.5% of the cells of the population have a tendency to migrate toward IL-8. 